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			<title>Medical Device Recalls since June 16, 2026</title>
			<description>U.S. Food and Drug Administration - Center for Devices and Radiological Health, Medical Device Class 1, 2 and 3 Recalls </description>
			<link>http://www.fda.gov/MedicalDevices/Safety/RecallsCorrectionsRemovals/ListofRecalls/default.htm</link>
			<language>en-us</language>
			<lastBuildDate>Sat, 27 Jun  2026 09:15:44 GMT</lastBuildDate>
			<webMaster>webmail@oc.fda.gov</webMaster>
			<image>
				<url>http://www.fda.gov/graphics/mastheadart/centers/fda_mast_01.gif</url> 
				<title>U.S. Food and Drug Administration - Center for Devices and Radiological Health</title>
				<link>http://www.fda.gov/MedicalDevices/Safety/RecallsCorrectionsRemovals/ListofRecalls/default.htm</link> 
				<description>A recall is a correction or removal of a product that is defective, could be a risk to health, or is in violation of FDA regulations.</description> 
				<width>116</width> 
				<height>70</height>
			</image>
	
	
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Abiomed Impella CP Set with SmartAssist (10th Generation) - Class 1 Recall]]></title>
				<description><![CDATA[Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221251</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221251</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP - Class 1 Recall]]></title>
				<description><![CDATA[Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000434. Introducer Product Code: 1000434.]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220455</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220455</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP - Class 1 Recall]]></title>
				<description><![CDATA[Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220456</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220456</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Abiomed Impella CP Set with SmartAssist (10th Generation) - Class 1 Recall]]></title>
				<description><![CDATA[Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834.]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220457</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220457</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline Convenience Kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline Convenience Kits:   1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142;   2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220687</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220687</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline Convenience Kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline Convenience Kits:   1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890;   2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066;   3) OPEN HEART, Model Number: DYNJ9855016V;   4) OPEN HEART, Model Number: DYNJ9855016X]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220688</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220688</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline Convenience Kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline Convenience Kits:   1) OPEN HEART CDS, Model Number: CDS840144Q;   2) OPEN HEART, Model Number: CDS840150W;   3) OPEN HEART ADULT, Model Number: CDS840396AA;   4) CABG A CDS, Model Number: CDS982269N;   5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G;   6) OPEN HEART ACCESSORY CDS, Model Number: CDS984289L;   7) OPEN HEART A, Model Number: CDS985105Q;   8) OPEN HEART PART 2, Model Number: DYNJ901075R;   9) VPH OPEN HEART, Model Number: DYNJ902664L;   10) HEART A, Model Number: DYNJ903465I;   11) HEART, Model Number: DYNJ903822F;   12) OPEN HEART BASIC B, Model Number: DYNJ904311F;   13) SM OPEN HEART PACK A&amp;B, Model Number: DYNJ904749J;   14) OPEN HEART ANESTHESIA ICC-B, Model Number: DYNJ905567B;   15) SILVER CROSS OPEN HEART, Model Number: DYNJ906102K;   16) ANESTHESIA OPEN HEART, Model Number: DYNJ906225I;   17) OPEN HEART COMBO, Model Number: DYNJ907400F;   18) CARDIAC CABG B, Model Number: DYNJ908121C;   19) FS OPEN HEART, Model Number: DYNJ908308A;   20) OPEN HEART SUPPLEMENT, Model Number: DYNJ909116D;   21) MEM CARDIAC, Model Number: DYNJ9622573AP;   22) OPEN HEART A &amp; B PACK, Model Number: DYNJ9718008AT]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220686</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220686</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline Convenience Kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline Convenience Kits:   1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP;   2) DYNJ905503G, Model Number: CV ANESTHESIA - ROOM SET UP]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220685</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220685</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Datex-Ohmeda Inc - Giraffe, Panda - Class 1 Recall]]></title>
				<description><![CDATA[Giraffe Warmer with Integrated Resuscitation System (iRes), Panda Warmer with Integrated Resuscitation System (iRes) Product Identifiers: M1118179, M1112198  Impacted only if service blender M1091607-R was installed during the last Preventative Maintenance.]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220639</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220639</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Datex-Ohmeda Inc - Panda - Class 1 Recall]]></title>
				<description><![CDATA[Panda Freestanding Warmer, Infant Radiant Warmer Product Identifiers: 2063568-001  Impacted only if service blender M1091607-R was installed during the last Preventative Maintenance.]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220640</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220640</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Datex-Ohmeda Inc - Giraffe - Class 1 Recall]]></title>
				<description><![CDATA[Giraffe Stand-alone Infant Resuscitation System; Powered emergency ventilator (resuscitator)  Product identifiers: 2082663-001, 2082663-002, M1241424    Product impacted only if service blender M1091607-R was installed during the last Preventative Maintenance]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220638</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220638</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Impella CP Set with SmartAssist - Class 1 Recall]]></title>
				<description><![CDATA[Impella CP Set with SmartAssist. Product Codes: 1000080, 1000851, 0048-0014, 0048-0024-JP.]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220257</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220257</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220064</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220064</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2;  PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PNHS2;  PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PNHS2]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220113</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220113</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220305</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220305</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: ACCESS TRAY/GU-04020; PSI KIT: 8.5 FR/AK-09803-CDC; PSI KIT: 9 FR/AK-09903-CDC; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-09810-PCMH1; PSI KIT: 9 FR X 10 CM/ASK-09903-KH; PSI KIT: 9 FR X 10 CM/ASK-09903-PHP1; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-UPA; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-YNH; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09907-SL; PSI KIT: 8.5 FR X 4-1/8IN (10 CM)/NA-09803-CDC; PSI KIT: 9 FR X 4-1/8IN (10 CM)/NA-09903-CDC; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-ECL4; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-MGH3; MULTI-LUMEN/PSI KIT/AK-11142-SPCS; MAC KIT: 2-L 9 FR DISTAL X 11.5 CM/CDC-11242-1A; MULTI-LUMEN/PSI KIT/AK-11142-D; MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-11142-MGH4; MULTI-LUMEN/PSI KIT/NA-11242-CDC; MULTI-LUMEN/PSI KIT/AK-21142-SK; MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-LMDTG; MULTI LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-RH; MULTILUMEN/PSI KIT 9 FR X 11.5 CM/ASK-21242-IMC; MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/ASK-21242-LMDTG; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMD; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UU3; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-VCU; MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-1A; MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-X1A; MULTI-LUMEN/PSI KIT/AK-21242-CDC; 2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-FH4; MULTI LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-GH1; 2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-SUU; 2-L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-UPMC4; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UKL; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMF; MULTILUMEN/PSI KIT: 9 FR X 4 1/2 IN/ASK-21242-UR1; PSI KIT: 8.5 FR/AK-29803-CDC; PSI KIT: 9 FR/AK-29903-CDC; PSI KIT: 9 FR/AK-29907-CDC; PSI KIT: 8.5 FR X 4IN (10 CM)/ASK-09804-UN1; PSI KIT: 9 FR/ASK-09903-UM; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-LMDT; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-LMDTG; PSI KIT: 9 FR X 4 1/8 (10 CM)/ASK-29903-BID1; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-LMDTG; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UMD; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-UR1; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-X1A; PSI KIT: 8.5 FR X 10 CM/ASK-29803-ECL; PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-UPM3; PSI KIT: 9 FR X 10 CM/ASK-29903-ECL; PSI KIT: 9FR X 4IN (10 CM) ANTIMICROBIAL/ASK-29903-UPM3; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09907-TG1]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220302</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220302</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: ACCESS TRAY/ASK-04001-MC3]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220359</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220359</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F, AHDC KIT: 3L 12 FR X 16 CM/ASK-12123-UOC1, AHDC KIT: 3-L 12 FR X 16 CM/ASK-12123-UPM, AHDC KIT: 3L 12 FR X 20 CM/ASK-15123-UOC1, AHDC KIT: 3-L 12 FR X 20 CM/ASK-15123-UPM, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-P1A, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-XP1A, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-XPCN1A, AHDC KIT: 3-L 12 FR X 16 CM/CDC-12123-XPN1A, AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-P1A, AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XPCN1A, AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XPN1A, AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPCN1A, HEMODIALYSIS KIT 2L: 12 FR X 20CM AGB/AK-25122-CDC, HEMODIALYSIS KIT: 2-LUMEN 14 FR X 20 CM/AK-25142-F, HEMODIALYSIS KIT: 2L 12 FR X 6 IN/ASK-22122-MM1, HEMODIALYSIS KIT: 2L 12 FR X 6 IN/ASK-22122-MM2, AHDC KIT: 2L 14 FR X 15 CM/ASK-22142-UOC1, AHDC AGB KIT: 2-L 14 FR X 15 CM/ASK-22142-UPM, HEMODIALYSIS KIT: 2L 14 FR X 20 CM/ASK-25142-UNC1, AHDC KIT: 2L 14 FR X 20 CM/ASK-25142-UOC1, AHDC AGB KIT: 2L 14 FR X 20 CM/ASK-25142-UPM, HEMODIALYSIS KIT 2L: 14 FR X 25 CM AGB/ASK-26142-UNC1, HEMODIALYSIS KIT: 2LUMEN 12 FR X 16 CM/AU-22122-F, HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-1A, AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-XCN1A-U, AHDC AGB KIT: 2-L 12 FR X 16 CM/CDC-22122-XN1A, AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-XN1A-U, HEMODIALYSIS KIT 2L: 14 FR X 15 CM AGB/CDC-22142-1A, HEMODIALYSIS KIT: 2L 14 FR X 15 CM AGB/CDC-22142-XC1A, AHDC AGB KIT: 2-L 14 FR X 15 CM/CDC-22142-XCN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-XCN1A-C, AHDC AGB KIT: 2-L 14 FR X 15 CM/CDC-22142-XN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-XN1A-C, AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-XCN1A-U, AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-XN1A-U, HEMODIALYSIS KIT: 2L 12 FR X 13 CM AGB/CDC-23122-XU1A, HEMODIALYSIS KIT: 2L 12 FR X 20 CM AGB/CDC-25122-1A, HEMODIALYSIS KIT: 2L 12 FR X 20 CM AGB/CDC-25122-X1A, AHDC AGB KIT: 2-L 12 FR X 20 CM/CDC-25122-XCN1A, AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-XCN1A-U, AHDC AGB KIT: 2-L 12 FR X 20 CM/CDC-25122-XN1A, HEMODIALYSIS KIT: 2L 12 FR X 20 CM AGB/CDC-25122-XU1A, HEMODIALYSIS KIT 2L: 14 FR X 20 CM AGB/CDC-25142-1A, HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB/CDC-25142-XC1A, AHDC AGB KIT: 2-L 14 FR X 20 CM/CDC-25142-XCN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-XCN1A-C, AHDC AGB KIT: 2-L 14 FR X 20 CM/CDC-25142-XN1A, AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-XN1A-C, HEMODIALYSIS KIT: 2L 12 FR X 25 CM AGB/CDC-26122-1A, AHDC AGB KIT: 2-L 12 FR X 25 CM/CDC-26122-XCN1A, AHDC AGB KIT: 2-L 12 FR X 25 CM/CDC-26122-XN1A, HEMODIALYSIS KIT 2L: 14 FR X 25 CM AGB/CDC-26142-1A, HEMODIALYSIS KIT: 2L 14 FR X 25 CM AGB/CDC-26142-X1A, AHDC AGB KIT: 2-L 14 FR X 25 CM/CDC-26142-XCN1A, AHDC AGB KIT: 2-L 14 FR X 25 CM/CDC-26142-XN1A, HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-25122-F, AHDC AGB KIT: 2-L 12 FR X 16 CM/CDC-22122-XCN1A, LBCVC AGB KIT: 3-L 12 FR X 16 CM/CDC-22123-XCN1A, LBCVC AGB KIT: 3-L 12 FR X 20 CM/CDC-25123-XCN1A, LBCVC AGB KIT:3-L 12 FR X 20 CM/CDC-25123-XN1A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220306</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220306</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC; RA CATH KIT: 20 GA X 5 IN/ASK-04020-MW; ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM5; CATH SL 20 GA X 5 CM HYDROPHILIC/ASK-00520-JH; CATH S-L 20 GA X 5 CM HYDROPHILIC/ASK-00520-UHC; ARTERIAL LINE KIT: 20 GA x 5IN/ASK-00820-CL; RA CATH KIT: 20 GA X 8 CM X 12 CM/ASK-00820-WC; ARTERIAL CATHETERIZATION KIT/ASK-01218-HM; SAC KIT: 20 GA X 12CM/ASK-01220-HMH; ARTERIAL CATH KIT: 20GA X 12CM/ASK-01220-NWM; ARTERIAL CATH KIT: 20 GA X 12 CM/ASK-01220-UH; ARTERIAL CATH: 18 GA X 6 1/2IN/ASK-01618-AU; RA CATH KIT: 18 GA X 6 IN/ASK-01618-CL; ARTERIAL CATH KIT: 18 GA X 6 1/2 IN/ASK-01618-JH; ARTERIAL CATHETERIZATION KIT/ASK-01618-PH; ARTERIAL CATH KIT: 18 GA X 6 1/2IN/ASK-01618-RU; ARTERIAL CATH KIT: 18 GA X 6IN (16 CM)/ASK-04018-HF; ARTERIAL CATH KIT: 18 GA X 6 IN (16 CM)/ASK-04018-NS; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-ST; RA CATH KIT: 20 GA X 1 1/2 IN (3.81 CM)/ASK-04120-BGH; ART/VESS CATH KIT:20GAX4.45CM/20GAX12CM/ASK-04500-SM; ARTERIAL LINE KIT/ASK-04500-UCH; ARTERIAL LINE KIT/ASK-04510-EUH2; ARTERIAL LINE KIT: 20GA X 5IN (12CM)/ASK-04510-MS4; ARTERIAL LINE KIT/ASK-04510-UPM; ARTERIAL CATH KIT: 20GA X 5CM/SAC-00520-1A; ARTERIAL CATH KIT: 20GA X 5CM/SAC-00520-X1A; ARTERIAL CATH KIT: 22GA X 5CM/SAC-00522-1A ARTERIAL CATH KIT: 22 GA X 5CM/SAC-00522-X1A; ARTERIAL CATH KIT: 20GA X 8CM/SAC-00820-1A; ARTERIAL CATH KIT: 20GA X 8CM/SAC-00820-X1A; SAC KIT: 18 GA X 12CM/SAC-01218-1A; SAC KIT: 18 GA X 12CM/SAC-01218-X1A; SAC KIT: 20 GA X 12CM/SAC-01220-1A; SAC KIT: 20 GA X 12CM/SAC-01220-X1A; SAC KIT: 18 GA X 16CM/SAC-01618-1A; SAC KIT: 18 GA X 16CM/SAC-01618-X1A; ACCESS TRAY/UM-04018; RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-ABM; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-BGH; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-LOL; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-MHS; RA CATH KIT: 20 GA X 1 3/4IN (4.45 CM)/ASK-04020-MIB3; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-PMC1; RA CATH SET: 20 GA X 1 3/4 IN/ASK-04020-URMC; RA CATH KIT: 20 GA X 1 1/2 IN (3.81 CM)/ASK-04220-FMH1; RA CATH KIT: 20 GA X 4.45 CM/NA-04020-1A; RA CATH KIT: 20 GA X 4.45 CM W BIO/NA-04020-B; RA CATH KIT: 20 GA X 4.45 CM W CHG/NA-04020-C; VESSEL CATH KIT: 20 GA X 5IN (12 CM)/ASK-04550-NYP; CVC KIT: 16 GA X 8 IN (20 CM)/ASK-04300-PHP1; CVC KIT: 16 GA X 8 IN (20 CM)/ASK-04301-TJ; ARTERIAL ACCESS KIT/ASK-04001-VAMC1; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-WBH]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220344</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220344</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB;  AGBA PICC G4 Stylet: 3L 6FR x 55CM TCG/DLX-45563-VPSC;  ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHD1;  ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UCHS1;  ARROW(R) VPS(R) ACCESS KIT/ASK-04001-DU13;  ARROW(R) VPS(R) ACCESS KIT/ASK-04001-UNHS1]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220033</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220033</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC; AGBA PICC: 2L 5.5 FR X 45 CM/ASK-44552-ABKB; AGBA PICC/DELTA KIT: 5.5 FR X 55 CM/ASK-45552-MHBV; AGBA PICC: 1L 4.5FR x 55CM w Biopatch/DLX-45541-HPKB; PICC/DELTA KIT: 2L 5.5 FR X 50 CM/ASK-45052-MC; AGBA PI PICC KIT: 1L 4.5FR 40CM/CDC-44041-HPK1A; AGBA PI PICC KIT 2-LUMEN: 5.5 FR X 40CM/CDC-44052-HPK1A; AGBA PICC/DELTA FG: 2-L 5.5 FR X 40 CM/CDC-44052-VPS2; PI AGBA PICC KIT: 3-L 6 FR X 50 CM/CDC-45063-HPK1A; AGBA PICC/DELTA KIT: 1-L 4.5 FR X 55 CM/CDC-45541-VPS2; AGBA PICC/DELTA FG: 2-L 5.5 FR X 55 CM/CDC-45552-VPS2; PICC/VPS 1L 4.5 FR/ASK-45541-CHS; PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI2; PICC KIT: 2L 5.5FR 55CM AGBA VPS/ASK-45552-CHS; PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI2; PICC KIT: 3L 6FR 55CM AGBA/ASK-45563-CHS; PI JACC KIT: 3L 6 FR X 25 CM CG+/ASK-42563-LTAC; PI JACC KIT: 1-L 4.5 FR X 25 CM CG+/CDC-42541-JX1A; PI JACC KIT: 2-L 5.5 FR X 25 CM CG+/CDC-42552-JX1A; PI JACC KIT: 3-L 6 FR X 25 CM CG+/CDC-42563-JX1A; PI JACC KIT: 2-L 5.5 FR X 30 CM CG+/CDC-43052-JX1A; PI JACC KIT: 3-LUMEN: 6 FR X 30 CM CG+/CDC-43063-JX1A; PICC KIT: 2-L 4 FR X 55 CM/CDC-05542-PK1A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220234</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220234</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: DRAINAGE KIT/AK-01600, DRAINAGE KIT/AK-01601, DRAINAGE KIT/ASK-01601-MM, THORACENTESIS KIT/AK-01000-T, THORACENTESIS KIT/AK-01000, THORACENTESIS KIT/ASK-01000-CHP, DRAINAGE KIT/ASK-01000-NW, THORACENTESIS KIT/ASK-01000-UPMS, PNEUMOTHORAX KIT/AK-01500, PNEUMOTHORAX KIT (NO HEIMLICH VALVE)/ASK-01500, PNEUMOTHORAX KIT/ASK-01500-JCM]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220262</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220262</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC;  AHDC KIT: 3-L 12 FR X 20 CM/AK-15123-PCDC;  AHDC KIT: 3-L 12 FR X 20 CM/CDC-15123-XP1A;  AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XP1A;  AHDC KIT: 3-L 12 FR X 25 CM/CDC-16123-XPN1A;  AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-XN1A-U;  LBCVC AGB KIT: 3-L 12 FR X 16 CM/CDC-22123-XN1A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220112</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220112</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB; SPINAL ANESTHESIA KIT/ASA-24103-SB; SPINAL ANESTHESIA KIT/ASA-25090-SB; SPINAL ANESTHESIA KIT: 24 GA X 9 CM/ASK-24090-SA; SPINAL ANESTHESIA KIT: 25 GA X 9 CM/ASK-24090-SPH; SPINAL ANESTHESIA KIT/ASK-25090-BIDMC; SPINAL ANESTHESIA KIT/ASK-25090-UF]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220341</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220341</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH, ASK-09458-COC, ASK-09458-EUH, ASK-09458-SD, ASK-09458-VU]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220009</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220009</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F;  HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122;  HEMODIALYSIS KIT 2L: 14 FR X 15CM AGB/AK-22142-CDC;  HEMODIALYSIS KIT 2L: 14 FR X 20CM AGB/AK-25142-CDC;  HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UMD;  HEMODIALYSIS KIT: 2L 14 FR X 15 CM/ASK-22142-UNC;  HEMODIALYSIS KIT: 2L 14 FR X 20 CM/ASK-25142-UMD;  HEMODIALYSIS KIT 2L: 14 FR X 20 CM AGB/ASK-25142-UN1;  HEMODIALYSIS KIT: 2L 14 FR X 25 CM/ASK-26142-UMD;  HEMODIALYSIS KIT: 2LUMEN 12 FR X 13 CM/AU-23122-F;  HEMODIALYSIS KIT: 2LUMEN 12 FR X 20 CM/AU-25122-F;  HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-X1A;  HEMODIALYSIS KIT: 2L 12 FR X 16 CM AGB/CDC-22122-XU1A;  HEMODIALYSIS KIT: 2L 14 FR X 15 CM AGB/CDC-22142-X1A;  HEMODIALYSIS KIT: 2L 12 FR X 25 CM AGB/CDC-26122-X1A;  HEMODIALYSIS KIT 2L: 12 FR X 16CM AGB/AK-22122-CDC;  HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-22122-F;  HEMODIALYSIS KIT: 2-LUMEN 14 FR X 15 CM/AK-22142-F;  AHDC AGB U-BEND KIT: 2-L 12 FR X 16 CM/CDC-22122-CN1AU;  AHDC AGB CURVED KIT: 2-L 14 FR X 15 CM/CDC-22142-CN1AC;  AHDC AGB U-BEND KIT: 2-L 12 FR X 13 CM/CDC-23122-CN1AU;  AHDC AGB U-BEND KIT: 2-L 12 FR X 20 CM/CDC-25122-CN1AU;  AHDC AGB CURVED KIT: 2-L 14 FR X 20 CM/CDC-25142-CN1AC;]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220065</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220065</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220260</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220260</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  ACCESS TRAY/ASK-04001-SUH-S;  ACCESS TRAY/ASK-04001-VM1;  STIMUCATH SFTY KIT: 19G CTH, 17Gx4CM NDL/AB-19604-KS;  STIMUCATH SFTY KIT: 19G CTH, 17Gx8CM NDL/AB-19608-KS;  STIMUCATH SFTY KIT: 20G CTH, 18Gx8CM NDL/AB-20608-KS;  STIMUCATH KIT: 19G CATH, 17G x 9CM NDL/AB-05060-PK;  FLEXBLOCK ULTRASOUND KIT: 17Gx9CM NS NDL/ASK-19609-VCU;  CONTINUOUS NERVE BLOCK KIT/ASK-19600-CC2;  CONTINUOUS NERVE BLOCK KIT 19 GA X 60/ASK-19608-CC;  CONTINUOUS NERVE BLOCK KIT 19GA X 60CM/ASK-19608-KP;  CONTINUOUS NERVE BLOCK KIT 19GA X 60CM/ASK-19608-SHC;  FLEXBLOCK KIT:ECHO CATH, 17Gx8CM STM NDL/FB-19608-K;  FLEXBLOCK ULTRASOUND KIT: 17Gx8CM STM ND/FB-19608-KU;  FLEXBLOCK KIT:ECHO CATH, 17Gx9CM NS NDL/FB-19609-K;  FLEXBLOCK ULTRASOUND KIT: 17Gx9CM NS NDL/FB-19609-KU;  CONTINUOUS PERIPHERAL NERVE BLOCK KIT/ASK-19608-US1;  EPIDURAL CATHETERIZATION KIT/ASK-05001-SLR1;  EPIDURAL CATHETERIZATION KIT/MH-05001;  EPIDURAL CATHETERIZATION KIT/WJ-05401;  SPINAL ANES/EPIDURAL CATH 19GA X 90CM/ASK-05501-USC1;  EPIDURAL NEEDLE KIT/LG-03000;  EPIDURAL ANESTHESIA KIT/MTO-03000-VM;  EPIDURAL ANESTHESIA KIT/SM-03001;  Anesthesia conduction kit/FB-19611-K]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220008</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220008</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC; PI JACC KIT: 3L 6 FR X 20 CM CG+/ASK-42063-LTAC; AGBA PI JACC KIT: 1-L 4.5 FR X 15 CM/CDC-41541-JX1A; AGBA PI JACC KIT: 2-L 5.5 FR X 15 CM/CDC-41552-JX1A; AGBA PI JACC KIT: 3-L 6 FR X 15 CM/CDC-41563-JX1A; AGBA PI JACC KIT: 1-L 4.5 FR X 20 CM/CDC-42041-JX1A; AGBA PI JACC KIT: 2-L 5.5 FR X 20 CM/CDC-42052-JX1A; AGBA PI JACC KIT: 3-L 6 FR X 20 CM/CDC-42063-JX1A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220259</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220259</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH;  PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU4;  PSI/CVC KIT: 9 FR/7 FR X 6IN (16CM)/ASK-09903-AMC1;  PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-CMC1;  PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU4;  PSI KIT: 9 FR X 4 1/8 IN (10CM)/ASK-09903-PCMH1;  PSI KIT: 8.5 FR X 10 CM/CDC-09803-1A;  PSI KIT: 9 FR X 4 IN (10 CM)/ASK-09903-ECL3;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-11242-PHP2;  MULTI LUMEN/PSI KIT/ASK-11142-NSU;  MULTI-LUMEN/PSI KIT/AK-21242-X;  MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-DMC;  MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-GMC1;  MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-HF5;  MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-LMDT;  2L MAC KIT: 9 FR DISTAL X 4IN (10 CM)/ASK-21142-UCL1;  2-L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-UPMC2;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-SL1;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UMH;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UN1;  MAC KIT: 2-L 9 FR DISTAL X 10 CM AGB/CDC-21142-XCN1A;  MAC KIT: 2-L 9 FR DISTAL X 10 CM AGB/CDC-21142-XN1A;  MAC KIT: 2-L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-XCN1A;  MAC KIT: 2-L 9 FR DISTAL X 11.5 CM AGB/CDC-21242-XN1A;  2L MAC KIT: 9 FR DISTAL X 4 IN/ASK-21142-CO1;  2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-FH3;  2L MAC KIT: 9 FR DISTAL X 4 IN (10 CM)/ASK-21142-OHSU3;  MULTILUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-SG2;  MULTILUMEN/MAC KIT: 9 FR X 4 IN (10 CM)/ASK-21142-UOI1;  2 LUMEN/PSI KIT: 9 FR X 4 IN (10 CM)/ASK-21142-WHC2;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-BID1;  AGB MAC KIT: 2L 9 FR DISTAL/ASK-21242-BSWH2;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-DU1;  MULTILUMEN/PSI KIT 9 FR X 11.5 CM/ASK-21242-PCMH1;  MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UCH2;  AGB MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-21242-UHC2;  PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/ASK-29803-BSWH2;  PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-HHC;  PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-MCY1;  PSI KIT: 8.5 FR X 4 IN (10 CM)/ASK-29803-UPM1;  PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29804-VCU;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-MCY1;  PSI KIT: 9 FR/ASK-29903-MHI;  PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-OHU4;  PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-UCH2;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UCL1;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-UHC4;  PSI KIT: 9FR X 4IN (10 CM) ANTIMICROBIAL/ASK-29903-UPM1;  PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-29907-LGH;  PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-1A;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-1A;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-X1A;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-XCN1A;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/CDC-29903-XN1A;  PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-AHH;  PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-XN1A;  PSI ACCESS TRAY/ASK-04001-MM2;  MAC KIT: 2L 9 FR DISTAL X 10 CM AGB/ASK-21142-GMC;  MULTI LUMEN/PSI KIT: 9 FR DISTAL X 4 1/2/ASK-21242-OSU3]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220052</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220052</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1;  RA CATH KIT: 20 GA X 1 1/2IN/NA-04220-S1A;  ARTERIAL LINE KIT/AK-04510-S;  ARTERIAL CATH KIT: 18 GA X 6IN (16 CM)/ASK-04018-HUMC;  ARTERIAL LINE KIT: 18 GA X 6 IN (16 CM)/ASK-04018-OH1;  RA CATH KIT: 20 GA X 1 3/4IN (4.45 CM)/ASK-04020-BID;  RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-MAR;  ARTERIAL LINE KIT: 20 GA X 5 IN/ASK-04020-PM4;  RA CATH KIT: 20 GA X 1 1/2IN (3.81 CM)/ASK-04120-HF3;  RA CATH SET: 20 GA X 2 1/2 IN (6.35 CM)/ASK-04120-UR;  ARTERIAL CATH KIT: 20 GA X 3 1/16 IN/ASK-04125-MGH;  ARTERIAL CATH KIT: 20 GA X 5 IN/ASK-04500-HFH4;  ARTERIAL LINE KIT: 20GA X 5IN/ASK-04510-BID2;  ARTERIAL LINE KIT: 20GA X 5IN (12 CM)/ASK-04510-EHP1;  ARTERIAL LINE KIT/ASK-04510-FEM1;  ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-HFH;  ARTERIAL CATH KIT: 20 GA X 5 IN/ASK-04510-HFH4;  ARTERIAL LINE KIT/ASK-04510-SE;  ARTERIAL LINE KIT: 20 GA X 5 IN (12CM)/ASK-04510-TGH2;  RA CATH KIT: 20 GA X 12 CM/NA-04550-1A;  RA CATH KIT: 20 GA X 12 CM/NA-04550-X1A;  RA CATH KIT: 18 GA X 1-3/4IN/AK-04018;  RA CATH KIT: 20 GA X 1-3/4IN/AK-04020;  RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-C;  RA CATH KIT: 20 GA X 1-1/2IN/AK-04120;  RA CATH KIT: 22 GA X 1-3/8IN/AK-04122;  RA CATH KIT: 20 GA X 1-1/2IN/AK-04220;  RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-AH;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-ATH;  RA CATH KIT: 20 GA X 1 3/4IN (4.45CM)/ASK-04020-AU2;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-BHS;  ARTERIAL CATHETERIZATION KIT/ASK-04020-BIDB2;  RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-CCD1;  ARTERIAL CATHETERIZATION KIT/ASK-04020-CR;  ART LINE KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-EUH2;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-FAM1;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-FMC;  RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-KSF2;  RA CATH KIT: 20 GA X 1 3/4 IN (4.5 CM)/ASK-04020-LHC2;  RA CATH KIT: 20 GA X 1 3/4 IN (4.5 CM)/ASK-04020-LHC3;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-LM;  RA CATH KIT: 20 GA X 1 3/4IN/ASK-04020-MCH1;  RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MIH1;  RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-NWMX;  RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-PHP;  RA CATH KIT: 20 GA X 1-3/4 IN (4.45CM)/ASK-04020-RIHM;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-RMC1;  RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-RU;  RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-SE;  RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-SHM;  RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-SRMC1;  RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-UCL1;  RA CATH KIT: 20 GA X 4.45 CM/ASK-04020-UMI;  RA CATH KIT: 20 GA X 1-3/4 IN (4.45CM)/ASK-04020-UN;  RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-UNC;  RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-UNC1;  RA CATH SET: 20 GA X 1-1/2IN (3.81CM)/ASK-04220-PSU;  RA CATH KIT: 20 GA X 1-1/2 IN (3.81 CM)/ASK-04220-UCL1;  RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-S1A;  CVC KIT: 20 GA X 5 IN (12CM)/ASK-04550-JMC1;  ARTERIAL ACCESS TRAY/ASK-04001-BW2;  ARTERIAL ACCESS TRAY WITH .025 IN SWG/ASK-04001-WUH1;  ARTERIAL LINE KIT/ASK-04510-HUM]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220035</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220035</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-09803-OSU5; PSI KIT: 8.5 FR/ASK-09807-UC; PSI KIT: 9 FR X 4 1/8IN (10 CM)/ASK-09903-HH2; PSI KIT: 9 FR X 10 CM/ASK-09903-LMDTG; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-09903-OSU5; PSI KIT: 9 FR X 10 CM/CDC-09903-1A; MAC KIT: 2L 9 FR DISTAL X 11.5 CM/ASK-11242-KSF2; MAC TWO LUMEN/PSI KIT: 9 FR X 11.5 CM/ASK-11242-KSF1 AGB MAC KIT: 2L 9 FR DISTAL/ASK-21242-MCY1; MULTI LUMEN PSI KIT: 9 FR DISTAL X 4 1/2/ASK-21242-OSU4; MAC KIT: 2-L 9 FR DISTAL X 11.5 CM/ASK-21242-UCD1; 2L MAC KIT: 9 FR DISTAL X 4 IN/ASK-21142-HHC MAC KIT: 2L 9 FR DISTAL X 11.5 CM AGB/ASK-21242-LMDT; PSI KIT: 8.5 FR X 4IN (10 CM)/ASK-09804-CCH; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29803-MM2; PSI KIT: 9 FR X 4 1/8 IN (10 CM)/ASK-29903-DU1; PSI KIT: 9 FR X 4 IN (10 CM)/ASK-29903-HHC; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-LMDT; PSI KIT: 9 FR X 4 1/8 (10 CM)/ASK-29903-NWM; PSI KIT: 9 FR X 10 CM ANTIMICROBIAL/ASK-29903-SL1; PSI KIT: 8.5 FR X 10 CM ANTIMICROBIAL/CDC-29803-XCN1A; PSI KIT: 8.5 FR X  4 1/8 IN (10 CM)/ASK-29803-HF6; PSI KIT: 8.5 FR X 4 1/8 IN (10 CM)/ASK-29804-HHN1; MULTI LUMEN/MAC KIT: 9 FR X 4 IN (10 CM)/ASK-21142-YWH;]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220360</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220360</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B; SAC KIT: 18 GA X 12CM W CHG/SAC-01218-C; SAC KIT: 18 GA X 16CM W BIO/SAC-01618-B]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220343</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220343</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A; AM/AT PI MIDLINE 1L: 4.5FR X 15CM/CDC-41541-MPK1A; AM/AT PI MIDLINE 2L: 5.5FR X 15CM/CDC-41552-MPK1A; AGBA PI MIDLINE 1L: 4.5FR X 15CM/ASK-41541-VFHM; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPK; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPKB; AGBA PI MIDLINE 1-L: 4.5FR X 15CM/CDC-41541-MPKC; AGBA PI MIDLINE 2-L: 5.5FR X 15CM/CDC-41552-MPK; AGBA PI MIDLINE 2-L: 5.5FR X 15CM/CDC-41552-MPKB; AGBA PI MIDLINE 2-L: 5.5FR X 15CM/CDC-41552-MPKC; PI MIDLINE 1-L: 4FR X 20CM/CDC-32041-MPK; PI MIDLINE 1-L: 4FR X 20CM/CDC-32041-MPKB; PI MIDLINE 1L: 4FR X 20CM/CDC-32041-MPKC; PI MIDLINE 2-L: 5FR X 20CM/CDC-32052-MPKB; PI PICC NaviCurve: 1L 4FR x 55CM w BP/DLX-35541-CURVB; PI PICC: 1L 4FR x 55CM w Biopatch/DLX-35541-HPKB; PI PICC: 1L 4FR x 55CM w CHG/DLX-35541-HPKC; PI PICC: 2L 5FR x 55CM w Biopatch/DLX-35552-HPKB; PI PICC: 2L 5FR X 55CM w CHG/DLX-35552-HPKC; PI PICC: 3L 6FR x 55CM w Biopatch/DLX-35563-HPKB; AGBA PICC/DELTA KIT: 1L 4.5 FR X 40 CM/ASK-44041-NS; AGBA PICC/DELTA FG: 2L 5.5 FR X 40 CM/ASK-44052-NS; AGBA PICC/DELTA KIT: 1L 4.5 FR X 50 CM/ASK-45041-NS; PI PICC KIT: 2L 5.5 FR X 50 CM/ASK-45052-TG; PI AGBA PICC KIT: 3L 6 FR X 50 CM W/VPS/ASK-45063-NS; PICC KIT: 1L 4.5 FR X 55 CM CG+ VPS/ASK-45541-RH; AGBA PICC: 1L 4.5FR x 55CM w Teg CHG/DLX-45541-HPKC; AGBA PICC: 2L 5.5FR x 55CM w Teg CHG/DLX-45552-HPKC; AGBA PICC NaviCurve: 3L 6FR x 55CM TCG/DLX-45563-CURVC; AGBA PICC: 3L 6FR x 55CM w Biopatch/DLX-45563-HPKB; AGBA PICC: 3L 6FR x 55CM w Teg CHG/DLX-45563-HPKC; PI PICC KIT: 1-L 4 FR X 55 CM TIPTRACKER/CDC-35541-TTS; PI PICC NaviCurve: 1L 4FR x 55CM w CHG/DLX-35541-CURVC; PI PICC G4 Stylet: 1L 4FR x 55CM w BP/DLX-35541-VPSB; PI PICC NaviCurve: 2L 5FR x 55CM w CHG/DLX-35552-CURVC; PI PICC G4 Stylet: 2L 5FR x 55CM w BP/DLX-35552-VPSB; PI PICC G4 Stylet: 2L 5FR x 55CM w CHG/DLX-35552-VPSC; PI PICC NaviCurve: 3L 6FR x 55CM w CHG/DLX-35563-CURVC; PI PICC G4 Stylet: 3L 6FR x 55CM w CHG/DLX-35563-VPSC; AGBA PICC/DELTA KIT: 1-L 4.5 FR X 40 CM/CDC-44041-VPS2; PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UWH1; PI AGBA PICC KIT: 2L 5.5FR X 55CM W/ VPS/ASK-45552-UWH1; AGBA PICC G4 Stylet: 1L 4.5FR x 55CM BP/DLX-45541-VPSB; ACCESS TRAY/ASK-04001-NWM; ACCESS TRAY/ASK-04001-VCUH3; PI PICC:1L 4FR X 40CM PRELOAD VPS STYLET/CDC-34041-VPS; PI PICC:2L 5FR X 50CM PRELOAD VPS STYLET/CDC-35052-VPS; ACCESS KIT/ASK-04001-BWK2; ARROW(R) VPS(R) ACCESS KIT/ASK-04001-DU11; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PVD; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16CM/ASK-12703-LMDTG1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8IN/ASK-15703-ECMC4; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-15703-PNM; CVC KIT: 3 LUMEN 12 FR X 6IN/ASK-22123-UAB; 2-L CVC KIT: 4 FR X13 CM/CDC-24402-X1A; LBCVC KIT: 3L 12 FR X 20 CM AGB/CDC-25123-X1A; CVC KIT: 3L 7 FR X 16 CM/ASK-42703-CPR; CVC KIT: 2L 8 FR X 6 IN (16 CM) AGB+/ASK-42802-DMC2; CVC KIT: 2 LUMEN 8 FR X 8 IN (20 CM)/ASK-45802-PCMH1; PI CVC KIT: 3L 7 FR X 6 IN (16 CM) AGB+/ASK-42703-MM1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PHUMC1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PMSG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 6/ASK-42703-POSU3; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PSAU1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-RHR1; PI CATHETER 2L: 8 FR X 16 CM AGB+/ASK-42802-DU1; PI CVC KIT: 2L 8 FR X 6 IN/ASK-42802-PHF4; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PHHN1; MULTILUMEN CVC KIT: 2L 8 FR X 6 IN/ASK-42802-POSU3; PI CVC KIT: 2-L 8 FR X 16 CM AGB+/ASK-42802-PUCD1; MULTI-LUMEN CVC KIT:2-L 8FR X 6IN (16CM)/ASK-42802-PWHC1; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-UHC; PI CVC KIT: 4L 8.5 FR X 16 CM AGB+/ASK-42854-MCY1; PI CVC KIT: 3L 7FR X 8IN (20 CM) AGB+/ASK-45703-BCH; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-EMC; PI CVC KIT: 3 LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-MHMC1; PI CVC KIT: 3-L 7 FR X 20 CM AGB+/ASK-45703-NWM; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PCOR; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PIMH; MULTI LUMEN CVC KIT: 3L]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220361</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220361</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS  AGBA PICC/DELTA: 2L 5.5 FR X 50 CM/ASK-45052-NS  AGBA PICC/DELTA KIT: 1L 4.5 FR X 55 CM/ASK-45541-MHBV  PICC KIT: 2L 5.5 FR X 55 CM CG+ VPS/ASK-45552-RH  AGBA PICC NaviCurve: 2L 5.5FR x 55CM BP/DLX-45552-CURVB  AGBA PICC NaviCurve: 2L 5.5FR x 55CM TCG/DLX-45552-CURVC  AGBA PICC: 2L 5.5FR x 55CM w Biopatch/DLX-45552-HPKB  AGBA PICC NaviCurve: 3L 6FR x 55CM BP/DLX-45563-CURVB  PI PICC KIT: 4 FR X 50 CM/ASK-35041-NH  PI PICC KIT: 2-L 5 FR X 50 CM/ASK-35052-NH  PI PICC G4 Stylet: 1L 4FR x 55CM w CHG/DLX-35541-VPSC  PI PICC NaviCurve: 2L 5FR x 55CM w BP/DLX-35552-CURVB  PI PICC NaviCurve: 3L 6FR x 55CM w BP/DLX-35563-CURVB  PI PICC G4 Stylet: 3L 6FR x 55CM w BP/DLX-35563-VPSB  AGBA PI PICC KIT: 2L 5.5 FR X 55CM/CDC-45552-HPK1A  PI AGBA PICC KIT: 3-L 6 FR X 55 CM/CDC-45563-HPK1A  PI AGBA PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-UOI1  PICC KIT: 1L 4.5 FR X 55 CM VPS/ASK-45541-VFH1  PI AGBA PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-UOI1  PICC KIT: 2L 5.5 FR X 55 CM VPS/ASK-45552-VFH1  PI AGBA PICC KIT: 3L 6 FR X 55 CM W/VPS/ASK-45563-UWH1  AGBA PICC NaviCurve: 1L 4.5FR x 55CM BP/DLX-45541-CURVB  AGBA PICC NaviCurve: 1L 4.5FR x 55CM TCG/DLX-45541-CURVC  AGBA PICC G4 Stylet: 1L 4.5FR x 55CM TCG/DLX-45541-VPSC  AGBA PICC G4 Stylet: 2L 5.5FR x 55CM BP/DLX-45552-VPSB  AGBA PICC G4 Stylet: 2L 5.5FR x 55CM TCG/DLX-45552-VPSC  PI PICC:1L 4FR X 50CM PRELOAD VPS STYLET/CDC-35041-VPS  PICC KIT: 3 FR X 55 CM/CDC-05531-PK1A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220062</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220062</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PARACENTESIS KIT/ASK-00376-JHH]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220304</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220304</guid>
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				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1;  EPIDURAL CATHETERIZATION KIT: 19 GA/AK-05501;  EPIDURAL CATHETERIZATION KIT/AK-05502;  EPIDURAL CATHETERIZATION KIT/AK-05502D;  EPIDURAL CATHETERIZATION KIT/AK-05503;  EPIDURAL CATHETERIZATION KIT/AK-05503-L;  SPINAL ANES/EPIDURAL CATH KIT/AK-05560;  SPINAL ANES/EPIDURAL CATH KIT/ASK-02520-SBMC1;  EPIDURAL CATHETERIZATION KIT/ASK-05400-BW1;  EPIDURAL CATHETERIZATION KIT/ASK-05400-GH;  SPINAL ANES/EPIDURAL CATH KIT/ASK-05401-LMC;  EPIDURAL CATHETERIZATION KIT/ASK-05401-NM;  SPINAL ANES/EPIDURAL CATH KIT/ASK-05500-BID1;  EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-JHH1;  EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-MCV1;  EPIDURAL CATHETER KIT: 19GA X 90CM ASK-05500-MVH;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-UMC;  19 GA X 35.5 IN EPIDURAL CATHETER KIT/ASK-05502-MLH;  SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-JMH1;  SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-MKD2;  SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-OM1;  EPIDURAL CATHETERIZATION KIT/ASK-17019-SM;  EPIDURAL CATHETERIZATION KIT/BP-05501;  EPIDURAL CATHETERIZATION KIT/CK-05401;  EPIDURAL CATHETERIZATION KIT/HS-05501;  EPIDURAL CATHETERIZATION KIT/MM-05501;  EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TK;  EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKD;  EPIDURAL CATHETERIZATION KIT: 19 GA/MP-17019-TKL;  EPIDURAL CATHETERIZATION KIT/MSO-05401-JMH;  EPIDURAL CATHETERIZATION KIT/NM-05401;  EPIDURAL CATHETERIZATION KIT/SJ-05501;  EPIDURAL CATHETERIZATION KIT/SM-05401;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/TM-05401;  EPIDURAL CATHETERIZATION KIT/TM-05502;  SPINAL ANES/EPIDURAL CATH KIT/UI-05502;  SPINAL ANES/EPIDURAL CATH KIT: 19 GA/ASK-05400-SHM;  EPIDURAL CATH KIT: 19 GA/ASK-05400-UOM;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05500-MR;  EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-05500-TM;  EPIDURAL CATHETERIZATION KIT/ASK-05501-BHL1;  EPIDURAL CATHETERIZATION KIT/ASK-05501-GH;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-SM;  EPIDURAL CATHETERIZATION KIT/ASK-05502-BSM;  EPIDURAL CATHETERIZATION KIT/ASK-05502-MGH1;  EPIDURAL CATHETERIZATION KIT/ASK-05503-BWB1;  EPIDURAL CATHETERIZATION KIT/ASK-05503-HMH;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-SPH;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05503-UPM1;  SPINAL ANES/EPIDURAL CATH KIT/ASK-05560-UCI2;  EPIDURAL CATHETERIZATION KIT: 19 GA/ASK-17019-UMP;  EPIDURAL CATHETERIZATION KIT/MH-05503-1;    EPIDURAL CATHETERIZATION KIT/ASK-05401-VB2;  Epidural Catheterization Kit: 19GA/ASK-05500-SC1;  Epidural Catheterization Kit: 19GA/ASK-05500-SC3;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-AFH1;  EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05501-BMC;  EPIDURAL CATHETERIZATION KIT/ASK-05502-NY;  EPIDURAL CATHETERIZATION KIT/ASK-17019-RMH]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220063</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220063</guid>
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			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: ACCESS TRAY/ASK-04001-JHH; ACCESS TRAY/ASK-04001-LMDTG; PI CVC KIT: 3 LUMEN 7 FR X 6 IN (16 CM)/ASK-12703-PSPH1; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-WMC2; MULTILUMEN PI CVC KIT: 3L 7 FR X 20CM/ASK-15703-LMDT1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20CM/ASK-15703-LMDTG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-15703-PVH; 1L CVC KIT: 16 GA X 8 IN (20CM)/ASK-24301-JHH1; CVC KIT: 16 GA X 16 CM/CDC-24306-1A; CVC KIT: 3-L 7 FR X 30 CM ANTIMICROBIAL/CDC-24703-X1A; LBCVC KIT: 3L 12 FR X 20 CM AGB/CDC-25123-1A; CVC KIT: 2L 8 FR X 6IN (16 CM)/ASK-42802-ECL3; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-ACH; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-BJC1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-DU1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-EMC; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6IN/ASK-42703-LMDT1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-LMDTG1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-MCY1; MULTILUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-NS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PAGP1; PI CVC KIT: 3L 7 FR X 6 IN (16 CM)/ASK-42703-PAM1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PAMC2; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PAU1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16/ASK-42703-PB1; PI CVC KIT: 3L 7 FR X 16CM AGB+/ASK-42703-PBSWH2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 16 IN/ASK-42703-PCAM1; MULTILUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-PCSJ2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PECL2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PGM4; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PHHN1; MULTI LUMEN CVC KIT: 3L 7 FR X 6 IN/ASK-42703-PLC; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PMEM; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PMHC1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-POHU2; MULTILUMEN PI CVC KIT: 3L 7 FR X 6/ASK-42703-POSU2; MULTILUMEN CVC KIT 7 FR X 6 IN (16 CM)/ASK-42703-PTJH; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PUCH2; PI CVC KIT: 3L 7 FR X 6 IN (16 CM) AGB+/ASK-42703-PUCI1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PUHC2; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PUMH; MULTI-LUMEN PI CVC KIT: 3-L 7 FR/ASK-42703-PUPM1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6 IN/ASK-42703-SHUF2; MULTI LUMEN PI CVC KIT: 3L 7 FR/ASK-42703-SL1; CVC KIT: 3 LUMEN 7 FR X 6 IN (16 CM)/ASK-42703-UMC; PI CVC KIT: 3L 7 FR X 6 IN (16 CM) AGB+/ASK-42703-WHH; CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-CHM; CVC KIT: 2L 8 FR X 16 CM/ASK-42802-LMDT1; PI CATHETER 2L: 8FR X 16CM AGB+/ASK-42802-MCY1; PI CVC KIT: 2L 8FR X 16CM AGB+/ASK-42802-PBSWH2; MULTILUMEN CVC KIT: 2L 8 FR X 6/ASK-42802-POSU2; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PUNCC2; PI CVC KIT: 2-L 8 FR/ASK-42802-PUPM1; PI CVC KIT: 2L 8 FR/ASK-42802-TGH1; PI CVC KIT: 4L 8.5 FR X 16 CM AGB+/ASK-42854-BJC1; CVC KIT: 4L 8.5 FR X (16CM) AGB+/ASK-42854-PBMH; PI CVC KIT: 4L 8.5FR X 16CM AGB+/ASK-42854-PMM; PI CVC KIT: 4L 8.5 FR X 16 CM AGB+/ASK-42854-PUCH2; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-ACH; 3L CVC KIT: 7 FR X 20 CM AGB+/ASK-45703-ARM; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-BJC1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-BLH; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-DU1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-HHC4; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-LMDT1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-LMDTG1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-MCY1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-NO; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-NS1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PADV1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PAGP1; MULTI LUMEN CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PAMC1; MULTI LUMEN CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PAU1; PI CVC KIT: 3L 7FR X 20CM AGB+/ASK-45703-PBSWH2; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PCAM1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PCSJ2; PI CVC KIT: 3L 7 FR X 8 IN (20 CM) AGB+/ASK-45703-PDM1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PECL2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/A]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220265</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220265</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X 1-3/4IN/NA-04020-X1ASP ACCESS TRAY/ASK-04001-MS RA CATH KIT: 20 GA X 8 CM/ASK-00820-UM1 VESSEL CATH KIT: 20GA X 5IN/AK-04550-S CVC KIT: 1-LUMEN 5 FR X 20 CM/AK-04301-SP CVC KIT: 16 GA X 6IN (16 CM)/AK-04306-SP CVC KIT: 16GA X 6 IN/AK-04800-S CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-12402 CVC KIT: 3-LUMEN 7 FR X 16 CM/AK-12703-CDC CVC KIT: 2L 4 FR X 13 CM/AK-14402 CVC KIT: 2-LUMEN 5 FR X 13 CM/AK-14502 CVC KIT: 3-LUMEN 5.5 FR X 30 CM/AK-14553 CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-14703-SP CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-15402 CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-15553 CVC KIT: 2-LUMEN 4 FR X 30 CM/AK-16402 CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-16553 CVC KIT: 5 FR X  20 CM/ASK-04301-HH2 CVC KIT 3L: 7 FR X 6 IN (16 CM)/ASK-12703-MGH3]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220177</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220177</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: CVC KIT: 16 GA X 8IN/AK-04210, CVC KIT: 1-L 16 GA X 8IN (20 CM)/AK-04300, CVC KIT: 14 GA X 6 IN/CK-04711]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220371</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220371</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220264</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220264</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-12123-F; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-15123-F; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PMAH; 3L PI CVC KIT: 7 FR X 16 CM/ASK-12703-PNM; 3L CVC KIT: 7 FR X 16 CM/ASK-12703-PUMH; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-15703-PRH; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/CDC-15703-P1A; PI CVC KIT: 3-L 7 FR X 6IN (16 CM)/NA-12703-PCDC; PI CVC KIT: 3-L 7 FR X 8IN (20 CM)/NA-15703-PCDC; CVC KIT: 3-LUMEN 5.5 FR X 8 CM/AK-25553; 2-L CVC KIT: 4 FR X 5 CM/CDC-22402-X1A; 2-L CVC KIT: 5 FR X 5 CM/CDC-22502-X1A; 2-L CVC KIT: 4 FR X 8 CM/CDC-25402-X1A; 2-L CVC KIT: 5 FR X 8 CM/CDC-25502-X1A; 3-L CVC KIT: 5.5 FR X 8 CM/CDC-25553-X1A; 3-L CVC KIT: 5.5 FR X 13 CM/CDC-26553-X1A; CVC KIT 3L: 12 FR X 16 CM AGB/AK-22123-CDC; CVC KIT: 3-LUMEN 12 FR X 16 CM/AK-22123-F; CVC KIT: 2-LUMEN 4 FR X 5 CM/AK-22402; CVC KIT: 2-LUMEN 5 FR X 5 CM/AK-22502; CVC KIT: 16 GA X 8IN/AK-24301-SK; CVC KIT: 2-LUMEN 4 FR X 13 CM/AK-24402; CVC KIT: 3-LUMEN 7 FR X 30 CM/AK-24703-ASK; CVC KIT 3L: 12FR X 20 CM AGB/AK-25123-CDC; CVC KIT: 3-LUMEN 12 FR X 20 CM/AK-25123-F; CVC KIT: 2-LUMEN 4 FR X 8 CM/AK-25402; CVC KIT: 2-LUMEN 5 FR X 8 CM/AK-25502; CVC KIT: 3-LUMEN 5.5 FR X 13 CM/AK-26553; LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-1A; LBCVC KIT: 3L 12 FR X 16 CM AGB/CDC-22123-X1A; CVC KIT: 16 GA X 20 CM/CDC-24301-1A; PI CVC KIT: 2L 7 FR X 16 CM AGB/AK-22702-P1A; PI CVC KIT: 2L 7 FR X 16 CM AGB/CDC-22702-XP1A; CVC KIT: 3L 7 FR X 20 CM/ASK-45703-CPR; MULTILUMEN PI CVC KIT: 3L 7 FR X 16 CM/ASK-42703-AKP1A; MULTI-LUMEN PI CVC KIT: 3-L 7 FR X 6IN/ASK-42703-KH; PI CVC KIT: 3L 7FR X 16CM AGB+/ASK-42703-MGH1; MULTI LUMEN PI CVC KIT: 3L 7 FR X 6IN/ASK-42703-PCCH2; PI CVC KIT: 3LUMEN 7 FR X 6IN (16 CM)/ASK-42703-PFS1; PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNO2; MULTI LUMEN PI CVC KIT: 3L 7 FR/ASK-42703-PSCH1; MULTILUMEN PI CVC KIT: 2L 8 FR X 16 CM/ASK-42802-AKP1A; CVC KIT: 2L 8 FR X 16CM/ASK-42802-LMDTG1; PI CVC KIT: 2L 8 FR X 6 IN (16 CM) AGB+/ASK-42802-PUCI1; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-PUMH; PI CVC KIT: 2L 8 FR X 16 CM AGB+/ASK-42802-UMM; PI CVC KIT: 4-L 8.5 FR X 6 IN/ASK-42854-AKP1A; PI CVC KIT: 4L 8.5FR X 16CM AGB+/ASK-42854-MGH; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-AKP1A; PI CVC KIT: 3L 7 FR X 20CM AGB+/ASK-45703-MGH; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PCCH2; MULTI LUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PECL1; PI CVC KIT: 3 LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PFS1; PI CVC KIT: 3L 7 FR X 8 IN (20 CM) AGB+/ASK-45703-PHM1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PHU; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PMSG1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PNCB; MULTILUMEN CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PPCM; PI CVC KIT: 3-LUMEN 7 FR X 8 IN (20 CM)/ASK-45703-PRH; MULTILUMEN PI CVC KIT: 3L 7 FR X 8 IN/ASK-45703-PSJ2; PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PSVM; MULTI LUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-PUHS; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-PUKL; PI CVC KIT: 3L 7FR X 20CM AGB+/ASK-45703-PUMF1; PI CVC KIT: 3L 7 FR X 8 IN (20 CM)/ASK-45703-PUR1; PI CVC KIT: 3L 7 FR X 20 CM AGB+/ASK-45703-RHR1; MULTILUMEN PI CVC KIT: 3L 7 FR X 20 CM/ASK-45703-WA; MULTI LUMEN PI CVC KIT: 2L 8 FR X 8 IN/ASK-45802-AKP1A; PI CVC KIT: 4L 8.5 FR X 20 CM/ASK-45854-AKP1A; PI CVC KIT: 4L 8.5FR X 20CM AGB+/ASK-45854-MGH; PI CVC KIT: 4L 8.5 FR X 8IN/ASK-45854-PCCH2; CVC KIT: 4L 8.5 FR X 20 CM AGB/ASK-45854-PNM; MULTI LUMEN CVC KIT: 4L 8.5 FR X 8 IN/ASK-45854-PPCM; PI CVC KIT: 4L 8.5 FR X 20 CM AGB+/ASK-45854-PUCH2; MULTILUMEN PI CVC KIT: 2L 7 FR X 20 CM/ASK-46702-PWBH1; MULTILUMEN CVC KIT: 2L 8 FR X 16 CM/CDC-42802-P1A; PI CVC KIT: 3-L 7 FR X 20 CM AGB/CDC-45703-PA1A; CVC KIT: 2L 8 FR X 6IN (16 CM)/ASK-42802-ECL4; PI CVC KIT: 3-L 7 FR X 16 CM AGB+/AK-42703-P1A; PI CVC KIT: 2-L 8 FR X 16 CM AGB+/AK-42802-P1A; PI CVC KIT: 4-L 8.5 FR X 16 CM AGB+/AK-42854-P1A; PI CVC KIT: 3-L 7 FR X 20 CM AGB+/AK-45703-P1A; PI CVC KIT: 2-L 8 FR X 20 CM AGB]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220116</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220116</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-UPM; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-HC; ARTERIAL LINE KIT: 20 GA X 5IN (12 CM)/ASK-04020-HMC; RADIAL ARTERY CATHETER KIT: 20 GA X 30MM/ASK-04020-MMC; RA CATH KIT: 20 GA X 1-1/2IN (3.81 CM)/ASK-04020-SV; ARTERIAL CATH KIT: 20 GA X 5 IN (12 CM)/ASK-04100-AMC-S1; ARTERIAL CATHETER KIT: 20 GA X 12 CM/ASK-04100-NS; RADIAL ARTERY KIT/ASK-04500-AH; RAD ART:20GAX3.81CM / ART LINE:20GAX12CM/ASK-04500-HF-S; ARTERIAL LINE KIT: 1L 20 GA X 12 CM/ASK-04510-HA; ARTERIAL LINE KIT: 20 GA. X 5 IN (12 CM)/ASK-04510-HF; ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-IHC1; ARTERIAL LINE KIT: 20 GA X 5 IN (12 CM)/ASK-04510-MSK2; ARTERIAL CATH KIT: 20GA X 5IN/ASK-04510-NS; ARTERIAL CATHETER KIT: 20 GA X 12 CM/FS-04510-S; ARTERIAL LINE KIT/HF-04510-1; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-BSM; RA CATH KIT: 20 GA X 1 3/4 IN (4.45CM)/ASK-04020-HH1; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-JMH1; RA CATH KIT: 20 GA X 1-3/4 IN/ASK-04020-MAS; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-MCC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MHT; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MI; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-MIHS; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-MUSC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-NCB; RA CATH KIT: 20 GA X 1 3/4 IN/ASK-04020-PMC; RA CATH KIT: 20 GA X 1-3/4IN (4.45 CM)/ASK-04020-SPH; RA CATH SET: 20 GA X 1-3/4IN (4.45CM)/ASK-04020-UPM; RA CATH KIT: 20 GA X 1 3/4 IN (4.45 CM)/ASK-04020-UR1; RA CATH KIT: 20 GA X 4.45 CM/NA-04020-X1A; RA CATH KIT: 20 GA X 1-3/4IN/WBH-04020-1; CVC KIT: 20 GA X 12CM/ASK-04510-UCLA; ARTERIAL ACCESS TRAY WITH .025IN SWG/ASK-04001-BW1]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220374</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220374</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220261</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220261</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF:  PACING PSI KIT: 6 FR/AI-06210-KS,  PACING PSI KIT: 5 FR 2-L/AI-07155-KS,  PACING PSI KIT: 5 FR 2L/ASK-07155-UPM]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220010</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220010</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[Description/REF: PICC ACCESS TRAY/ASK-04001-CG1]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220370</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220370</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARROW INTERNATIONAL, LLC - Arrow Kits and Sets that contain Lidocaine and Bupivacaine - Class 1 Recall]]></title>
				<description><![CDATA[PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU]]></description>
				<pubDate>Sun, 14 Jun 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219841</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219841</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Automated Impella Controller (AIC) - Class 1 Recall]]></title>
				<description><![CDATA[Automated Impella Controller (AIC), for use with left heart support blood pump.  Labeled as the following with corresponding Product Codes:     1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU.     2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA.     3. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU.    4. Impella Controller, Packaged, IN; Product Code: 0042-0000-IN.     5. Impella Controller, Packaged, JP; Product Code: 0042-0000-JP.     6. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK.     7. Impella Controller, Packaged, US; Product Code: 0042-0000-US.     8. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU.     9. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU.     10. Impella Optical Controller, Packaged, IN; Product Code: 0042-0010-IN.     11. Impella Optical Controller, Packaged, UK; Product Code: 0042-0010-UK.     12.Impella Optical Controller, Packaged, US, UK; Product Code: 0042-0010-US.     13. Optical AIC w/Impella Connect, Pack&apos;d, CA; Product Code: 0042-0040-CA.     14. Optical AIC w/Impella Connect, Pack&apos;d, EU; Product Code: 0042-0040-EU.     15. Optical AIC w/Impella Connect, Pack&apos;d, JP, EU; Product Code: 0042-0040-JP.     16. Optical, AIC, Impella Connect, Pkgd, AU; Product Code: 0042-0040-AU.    17. Optical, AIC, Impella Connect, Pkgd, UK; Product Code: 0042-0040-UK.    18. Optical, AIC, Impella Connect, Pkgd, US; Product Code: 0042-0040-US.]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:57 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219986</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219986</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Draeger, Inc. - Atlan anesthesia workstation - Class 1 Recall]]></title>
				<description><![CDATA[Atlan A350. Model Number: 8211500. anesthesia workstation]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220173</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220173</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Draeger, Inc. - Atlan A350XL anesthesia workstation - Class 1 Recall]]></title>
				<description><![CDATA[Atlan A350XL. Model Number: 8621600.  anesthesia workstation]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220174</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220174</guid>
			</item>
	
	
			<item>
				<title><![CDATA[KAYSERBETTEN GMBH &amp; CO. KG - KayserBett IDA - Class 1 Recall]]></title>
				<description><![CDATA[Pediatric care bed;  Product Designation: KayserBett IDA;]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219886</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219886</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B.Braun PENCAN - Class 1 Recall]]></title>
				<description><![CDATA[Spinal Needle procedure kits:   Material Description (Material Number)  24GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333867);  25GA. PENCAN SPINAL BUP. TRAY W/DURAPREP (333862);  GOVP24BK 24G PENCAN TRAY W/ BUP &amp; DEXTROS (332607);  P24BK 24G PENCAN TRAY W/BUP &amp; DEXTROSE (333868);  P25BKAY PENCAN SPINAL TRAY (333865);  P27BK PENCAN SPINAL W/BUPIVAC (333871);  P25BK SPINAL TRAY (333851)]]></description>
				<pubDate>Thu, 04 Jun 2026 01:07:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219939</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219939</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B.Braun Spinocan - Class 1 Recall]]></title>
				<description><![CDATA[Spinocan Spinal Needle procedure kits:   Material Description (Material Number):  Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201);  Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211);  Spinocan 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333231)]]></description>
				<pubDate>Thu, 04 Jun 2026 01:07:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219940</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219940</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B.Braun Spinocan - Class 1 Recall]]></title>
				<description><![CDATA[Design Options Spinal Tray Spinal Needle Anesthesia procedure kits:   Material Description (Material Number):  SSK H M C 20061890 (560074),  SSK S C H (560214),  SSK BJC H S (ORIGINAL CUST) (560272),  SSK CA P M C (ORIGINAL CUST) (560327),  SSK T M H (560394),  SSK S O 20070208 (560428),  SSK L G H (ORIGINAL CUST) (560462),  SSK H M H (560465),  SSK BUPIVACAINE TRAY 2068824 (560476),  SSK K F H (560497),  SSK T J U H (560513),  SSK O M C (560521),  SSK CUSTOM SPINAL TRAY (560523),  SSK O R M C (560533),  SSK B S H S 20115122 (560538),  SSK M M (560572),  SSK M S 27GA PENCAN SPINAL TRAY (560580),  SSK S T H &amp; C (560584),  SSK U C (560587), SSK P25BKG (560603),  SSK P24BKG (560606),  SSK S25BKG (560607),  SSK M C - BUPIVACAINE TRAY (560609),  SSK T M C (560613),  SSK PENCIL POINT SPINAL TRAY (560619),  SSK E O &amp; S H-SPINAL (560621),  SSK BSW SPINAL TRAY (560628),  SSK M C OB DEPT - SPINAL (560645),  SSK B H M (560646),  SSK M G M C (560647),  SSK S M H (560648),  SSK H H S (560660),  O S U M C SPINAL TRAY SSK (560667),  A M C, SSK (560670),  S B H - SPINAL TRAY SSK (560672);]]></description>
				<pubDate>Thu, 04 Jun 2026 01:07:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219942</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219942</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Fresenius Kabi USA, LLC - LVP software of the Ivenix Infusion System (IIS) - Class 1 Recall]]></title>
				<description><![CDATA[LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:49 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220229</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220229</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Fresenius Kabi USA, LLC - Ivenix Infusion System (IIS) - Class 1 Recall]]></title>
				<description><![CDATA[Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004]]></description>
				<pubDate>Sat, 30 May 2026 01:07:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220255</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220255</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 25 G x 3.5 in., BD&#xbf;Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405741.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219962</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219962</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219959</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219959</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405637, 405707.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219966</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219966</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400866, 405672, 405673, 405674, 405675, 405709, 405721, 405723, 406704.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219964</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219964</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Quincke Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 405621, 405735.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219958</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219958</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 24 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Numbers: 400868, 405652.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219961</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219961</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219960</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219960</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Quincke Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405609.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219957</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219957</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 2 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405658.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219963</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219963</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Company - BDSpinal Tray - Class 1 Recall]]></title>
				<description><![CDATA[BD&#xbf;Spinal Tray with BD&#xbf;Whitacre Needle 25 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405671.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219965</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219965</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Automated Impella Controller (AIC) - Class 1 Recall]]></title>
				<description><![CDATA[Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes.    1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA.     2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU.     3. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK.     4. Impella Controller, Packaged, US; Product Code: 0042-0000-US.]]></description>
				<pubDate>Fri, 29 May 2026 01:06:54 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220038</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220038</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:    1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A;   2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219931</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219931</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:    1) PAIN TRAY, Medline Kit SKU DYNJRA1555;   2) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1817;   3) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA1920;   4) ULTRASOUND GUIDED NERVE BLOCK, Medline Kit SKU DYNJRA2013;   5) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2017;   6) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2067;   7) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2067A;   8) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2093;   9) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2117A;   10) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2124;   11) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2124A;   12) PAIN TRAY, Medline Kit SKU DYNJRA2144;   13) TRAY, 24G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2221;   14) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2333;   15) SPINAL TRAY, Medline Kit SKU DYNJRA2390;   16) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2402;   17) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2407;   18) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2407A;   19) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2407B;   20) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2447;   21) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2447A;   22) SPINAL TRAY 25G, Medline Kit SKU DYNJRA2488A;   23) J&amp;S SPINAL TRAY, Medline Kit SKU DYNJRA2545;   24) SPINAL TRAY, Medline Kit SKU DYNJRA2549;   25) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2550;   26) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2552;   27) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2554;   28) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2554A;   29) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA2578;   30) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2588;   31) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2602;   32) SPINAL TRAY, Medline Kit SKU DYNJRA2618;   33) SPINAL TRAY, Medline Kit SKU DYNJRA2619;   34) SPINAL TRAY, Medline Kit SKU DYNJRA2622;   35) SPINAL BLOCK 25 WHITACRE 5S ND, Medline Kit SKU DYNJRA2624;   36) SPINAL TRAY, Medline Kit SKU DYNJRA2631;   37) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA2632;   38) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2633;   39) SPINAL TRAY, Medline Kit SKU DYNJRA2645;   40) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2654;   41) CSE PAIN MANAGEMENT TRAY, Medline Kit SKU DYNJRA2665;   42) SPINAL TRAY, Medline Kit SKU DYNJRA2667;   43) SPINAL TRAY 24G BD, Medline Kit SKU DYNJRA2675;   44) SPINAL TRAY W/ CHLORAPREP, Medline Kit SKU DYNJRA2680;   45) SPINAL TRAY, Medline Kit SKU DYNJRA2682;   46) TRAY, 24G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2684;   47) SPINAL TRAY, Medline Kit SKU DYNJRA2725;   48) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2757;   49) TRAY, 25G SPINAL W/RX DURAPREP, Medline Kit SKU DYNJRA9039;   50) TRAY, 25G SPINAL W/RX, Medline Kit SKU DYNJRA9045;   51) SLSYSTEM CSE TRAY, Medline Kit SKU PAIN2333;   52) 25G SPINAL BLOCK TRAY, Medline Kit SKU SAMPA0135.]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219932</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219932</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:  1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A;  2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B;  3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B;  4) SPINAL TRAY, Medline Kit SKU DYNJRA0255B;  5) SPINAL TRAY, Medline Kit SKU DYNJRA0320;  6) SPINAL TRAY, Medline Kit SKU DYNJRA0320A;  7) SPINAL BLOCK TRAY- LF, Medline Kit SKU DYNJRA0413C;  8) SPINAL TRAY, Medline Kit SKU DYNJRA0461D;  9) 25G SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA0945;  10) SPINAL TRAY, Medline Kit SKU DYNJRA1140B;  11) SPINAL TRAY, Medline Kit SKU DYNJRA1192;  12) SPINAL TRAY 25G, Medline Kit SKU DYNJRA1240;  13) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1288;  14) SPINAL 25G WHITACRE, Medline Kit SKU DYNJRA1301;  15) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA1304;  16) AHN SPINAL TRAY, Medline Kit SKU DYNJRA1376;  17) SPINAL TRAY, Medline Kit SKU DYNJRA1477A;  18) ADULT SPINAL KIT, Medline Kit SKU DYNJRA1538;  19) SPINAL TRAY, Medline Kit SKU DYNJRA1558A;  20) SPINAL TRAY, Medline Kit SKU DYNJRA1560A;  21) SPINAL TRAY, Medline Kit SKU DYNJRA1565;  22) SPINAL ANESTHESIA TRAY, Medline Kit SKU DYNJRA1577C;  23) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1584;  24) 25G WHITACRE SPINAL TRAY, Medline Kit SKU DYNJRA1740A;  25) SPINAL TRAY, Medline Kit SKU DYNJRA1744A;  26) SPINAL TRAY, Medline Kit SKU DYNJRA1750A;  27) SPINAL TRAY, Medline Kit SKU DYNJRA1784;  28) SPINAL TRAY, Medline Kit SKU DYNJRA1790;  29) SPINAL TRAY, Medline Kit SKU DYNJRA1796;  30) MSSC SPINAL TRAY, Medline Kit SKU DYNJRA1802B;  31) SPINAL TRAY, Medline Kit SKU DYNJRA1818;  32) SPINAL TRAY, Medline Kit SKU DYNJRA1839;  33) SPINAL TRAY, Medline Kit SKU DYNJRA1884;  34) SPINAL TRAY, Medline Kit SKU DYNJRA1884A;  35) 24G SPINAL KIT, Medline Kit SKU DYNJRA1889;  36) SPINAL TRAY, Medline Kit SKU DYNJRA1929;  37) SPINAL TRAY, Medline Kit SKU DYNJRA1969;  38) SPINAL TRAY, Medline Kit SKU DYNJRA1982;  39) SPINAL TRAY/PENCAN, Medline Kit SKU DYNJRA1983A;  40) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1987;  41) SPINAL TRAY - 3 ML CHLORAPREP, Medline Kit SKU DYNJRA2005;  42) SPINAL TRAY, Medline Kit SKU DYNJRA2023;  43) SPINAL TRAY, Medline Kit SKU DYNJRA2068A;  44) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2088;  45) 25G WHITACRE SPINAL TRAY, Medline Kit SKU DYNJRA2115;  46) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2117;  47) SPINAL TRAY, Medline Kit SKU DYNJRA2140;  48) SPINAL TRAY, Medline Kit SKU DYNJRA2153;  49) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA2213;  50) SPINAL TRAY, Medline Kit SKU DYNJRA2225;  51) OR SPINAL BLOCK KIT, Medline Kit SKU DYNJRA2349;  52) SPINAL TRAY, Medline Kit SKU DYNJRA2360;  53) L&amp;D SPINAL TRAY, Medline Kit SKU DYNJRA2371;  54) TRAY, 25G WHIT SPINAL W/PHARM, Medline Kit SKU DYNJRA2381;  55) SPINAL TRAY, Medline Kit SKU DYNJRA2432A;  56) OB SPINAL TRAY, Medline Kit SKU DYNJRA2532;  57) SPINAL TRAY, Medline Kit SKU DYNJRA2534;  58) SPINAL TRAY, Medline Kit SKU DYNJRA2556;  59) SPINAL TRAY, Medline Kit SKU DYNJRA2566A;  60) SPINAL TRAY BRAUN, Medline Kit SKU DYNJRA2575;  61) SPINAL TRAY, Medline Kit SKU DYNJRA2592;  62) SPINAL TRAY, Medline Kit SKU DYNJRA2597;  63) SPINAL BLOCK, Medline Kit SKU DYNJRA2605;  64) SPINAL TRAY, Medline Kit SKU DYNJRA2606;  65) SPINAL TRAY, Medline Kit SKU DYNJRA2607;  66) SPINAL TRAY, Medline Kit SKU DYNJRA2607A;  67) SPINAL TRAY, Medline Kit SKU DYNJRA2611;  68) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2613;  69) SPINAL TRAY, Medline Kit SKU DYNJRA2618A;  70) SPINAL TRAY, Medline Kit SKU DYNJRA2634;  71) SPINAL TRAY, Medline Kit SKU DYNJRA2638;  72) SPINAL TRAY, Medline Kit SKU DYNJRA2639;  73) JOI SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA2641;  74) SPINAL TRAY, Medline Kit SKU DYNJRA2653;  75) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA2669;  76) SPINAL TRAY, Medline Kit SKU DYNJRA2670;  77) SPINAL BLOCK TRAY 18G INTRO, Medline Kit SKU DYNJRA2672;  78) SPINAL TRAY 24G, Medline Kit]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219937</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219937</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:    1) BLOCK TRAY, Medline Kit SKU DYNJRA1181C;   2) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKu DYNJRA1860.]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219934</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219934</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:     1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097;   2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154;   3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A;   4) BLOCK TRAY, Medline Kit SKU DYNJRA1212;   5) SPINAL NEEDLE TRAY, Medline Kit SKU DYNJRA1285;   6) SPINAL BLOCK TRAY WHITACRE 24G, Medline Kit SKU DYNJRA9031;   7) SPINAL BLOCK TRAY 25G WHITACRE, Medline Kit SKU DYNJRA9032;   8) 25G SPINAL TRAY, Medline Kit SKU PAIN1239.]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219936</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219936</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:  SPINAL BLOCK 22G QUINCKE 5S BU, Medline Kit SKU DYNJRA9026]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219935</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219935</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 1 Recall]]></title>
				<description><![CDATA[Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as:   1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245;   2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555;   3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A;   4) SPINAL TRAY, Medline Kit SKU DYNJRA0978A;   5) TRAY, SPINAL, WHIT 24GX4, Medline Kit SKU DYNJRA1034;   6) SPINAL BLOCK 25G WHTCRE 5S BU, Medline Kit SKU DYNJRA9028;   7) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA9030.]]></description>
				<pubDate>Fri, 29 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219933</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219933</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas LP - BD 10ml Syringe LuerLok Tip - Class 2 Recall]]></title>
				<description><![CDATA[SYRINGE LUER LOK 10CC-200/BOX  BD Product Code: 302995  Mentor Product Code: B9604    Syringe, Piston]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220342</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220342</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    CABG A CDS    CDS982269K   CDS982269L   CDS982269M   CDS982269N     CARDIAC MAJOR    DYNJ901328D   DYNJ901328F     HEART A    DYNJ903465F   DYNJ903465G     HEART TRAY-VASCULAR    DYNJ907857   DYNJ907857A   DYNJ907857B     KIT UNIVERSITY CABG PK    DYNJ905857A     OPEN HEART    CDS981161AA   CDS981161AB   DYNJ905437A   DYNJ909090   DYNJ909090C   DYNJ9855016R   DYNJ9855016S     OPEN HEART ACCESSORY CDS    CDS984289J     OPEN HEART ANESTHESIA PACK    CDS983849D   CDS983849F   CDS983849G     OPEN HEART B CDS    DYNJ900377P     OPEN HEART BASIC B    DYNJ904311C     OPEN HEART CDS    CDS983513F     OPEN HEART CDS QVH    CDS982523K   CDS982523L   CDS982523N     OPEN HEART LINE SET UP    DYNJ908179   DYNJ908179A     OPEN HEART SUPPLEMENT    DYNJ909116   DYNJ909116A   DYNJ909116C   DYNJ909116D     SILVER CROSS OPEN HEART    DYNJ906102J   DYNJ906102K   DYNJ906102L        SM OPEN HEART PACK A&amp;B    DYNJ904749G   DYNJ904749J     VPH OPEN HEART    DYNJ902664J   DYNJ902664K   DYNJ902664L]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221068</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221068</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    CENTRAL AND ARTERIAL LINE TOTE    DYNJ8407]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221063</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221063</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    OPEN HEART    DYNJ909090B    OPEN HEART CDS QVH    CDS982523M]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221066</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221066</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    CARDIAC MAJOR    DYNJ901328G      HEART A    DYNJ903465K     OPEN HEART    DYNJ909090G     SILVER CROSS OPEN HEART    DYNJ906102M     VPH OPEN HEART    DYNJ902664M   DYNJ902664N]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221062</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221062</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    CV ANESTHESIA - ROOM SET UP    DYNJ905503D   DYNJ905503F   DYNJ905503G]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221065</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221065</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    KIT GERMANTOWN CABG    DYNJ905855     KIT UNIVERSITY CABG PACK    DYNJ905857     OH MED RN CDS    DYNJ905936B]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221064</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221064</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    RIGHT HEART CATH PACK CTX    DYNJ68530A]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221067</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221067</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline Convenience kits containing recalled Swan-Ganz Catheters    RIGHT HEART CATH PACK CTX    DYNJ68530B]]></description>
				<pubDate>Sat, 27 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221061</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221061</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Boston Scientific Corporation - Intera Oncology - Class 2 Recall]]></title>
				<description><![CDATA[Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220721</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220721</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    AAA    DYNJ905651B     ARTERIOGRAM TRAY    00-402001S     AV SHUNT PACK-LF    DYNJ0842516F     BASIC IR PACK-LF    PHS463660F     CATH PROCEDURAL TRAY    DYNJ43580C     CONGENITAL ADD-ON KIT    DYNDA2213A     CUSTOM PROCEDURE KIT    DYNJ65277A     DEEP BRAIN STIMULATION PACK    DYNJ0842793F     HOSPITAL REGIONAL DE CONCEPCIO    DYNJ67918     INTERVENTIONAL PACK    DYNJ56666B     INVASIVE LINE INSERTION    DYNJ44123A     JUDKINS PACK    DYNJ51126B     LARKIN CUSTOM NEURO TRAY    PAIN1454     MAJOR PLUS PACK    DYNJ905160I     MINIMALLY INVASIVE PACK-LF    DYNJ0843063J     NEURO ANGIO PACK SJF-LF    DYNJ37304F     NON-VASCULAR PACK    DYNJ56386B     OR HYBRID-MRMC    DYNJ907758     PACER PACK    DYNJ40952     PAIN PACK    DYNJ60715     PICC PHC    DYNJ37484B     ROBOTIC PACK    DYNJ908706A     THORACOTOMY PACK-LF    DYNJ0101339J   DYNJ69090     VENOUS PACK    DYNJ56260B]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220728</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220728</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    KIT NEURO CSTM    SAMP0551]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220741</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220741</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIOGRAM PACK-LF     DYNJ21574J     JUDKINS PACK     DYNJ51126]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220722</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220722</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIO CATH COMBINED PACK  DYNJ43609S    ANGIO PACK  DYNJ67987D  DYNJ80317A    ANGIO SPECIAL PROCEDURE-LF  DYNJ38412C    ANGIOGRAM SET UP PACK  DYNJ66260A    ANGIOGRAPHY PACK  DYNJ44293I    ANGIOGRAPHY PACK-LF  DYNJ0854485W    CARDIAC CATH PACK  DYNJ82709    CARDIAC CATH PACK-LF  DYNJ0261554AL  DYNJ31103F    CATH LAB ANGIO TRAY  DYNJ83506    CATH LAB PACK  DYNJ66366C    MSC-GREEN BAY ST VINCENT  SAMPC0686    NEUROLOGICAL CATH PACK  DYNJ63434B    OR HYBRID-MRMC  DYNJ907758B    STEWARD OR ANGIO PACK GSS  DYNJ80925B]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220723</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220723</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    CRANIOTOMY PACK-LF    DYNJ0101292F   DYNJ0101292G     HYBRID PACK    DYNJ65925A     LAMINECTOMY    DYNJ905156L   DYNJ905156M   DYNJ905156N   DYNJ905156O   DYNJ905156P     MAJOR EXTREMITY    DYNJ905159F   DYNJ905159I   DYNJ905159J   DYNJ905159K     NEURO CERVICAL PACK    DYNJ0101287J   DYNJ0101287K     NEURO SPINE PACK    DYNJ81612C     POSTERIOR SPINE PACK-LF    DYNJ0843339L   DYNJ0843339M   DYNJ0843339N     SPINE PACK    DYNJ30150F]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220739</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220739</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    FTMC C-SECTION TRAY-LF    DYNJ54603B]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220757</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220757</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ABDOMINAL VASCULAR-LF    DYNJ905291B   DYNJ905291C     ARTERIOGRAM    DYNJ28082G     CVICU HEART BAG    DYKM2130A     ENDOVASCULAR PACK    DYNJ0678934J     EP PACK    DYNJ23456J     GENERAL ENDO PACK-LF    DYNJ0842873K     HYBRID PACK    DYNJ65925B   DYNJ65925C     NON VASCULAR PACK    DYNJ68037     PACEMAKER    DYNJ901681D     PACEMAKER PACK    DYNJ51853C   DYNJ51853D   DYNJ60606A     PACER PACK    DYNJ40952A     RADIOLOGY VASCULAR ACCESS TRAY    DYNJVB1303A     SM- INTERVENTIONAL DRAPE PK-LF    DYNJ0780143K     VASCULAR ACCESS PACK-LF    DYNJ0101291D     VASCULAR DSC    DYNJ69172   DYNJ69172B    VASCULAR HYBRID    DYNJ57543F   DYNJ57543I   DYNJ57543J     VASCULAR PACK    DYNJ61702A]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220751</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220751</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    DR G&apos;S BREAST PACK    DYNJ51124B     LIPO SUPPLEMENT PACK-LF    DYNJ0341174D     PLASTIC PACK    DYNJ66746   DYNJ85702]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220727</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220727</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIOGRAPHY PACK-LF    DYNJ0854485S        DEEP BRAIN STIMULATION PACK    DYNJ0842793G      NEURO ACCESSORY PACK    DYNJ55385A     NEURO ANGIO PACK    DYNJ51697B   DYNJ56509G   DYNJ56509I   DYNJ68063   DYNJ68845   DYNJ68845A   DYNJ68845B     NEURO CERVICAL PACK    DYNJ0101287I   DYNJ0101287L     NEURO PACK    DYNJ82103   DYNJ82103A     NEURO TRAY    DYNJ67075   DYNJ67075A   DYNJ67075B     NEURO VASCULAR PACK    DYNJ62960B     NEURO VP SHUNT PACK-LF    DYNJ0843121J   DYNJ0843121K     NEUROLOGICAL CATH PACK    DYNJ63434A   DYNJ63434C     NEURORADIOLOGY PK    DYNJ40420D     RADIOLOGY ANGIO MAJOR PACK-LF    DYNJ62858A     RADIOLOGY NEURO DRAPE PAC    DYNJ61449     RRMC ANGIO PACK    DYNJ36338B]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220729</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220729</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    PICC LINEPACK (PCLUI)642-LF    DYNJ47717A]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220755</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220755</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    MAJOR BASIN SET    DYNJ85723]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220740</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220740</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    BARIATRIC  DYNJ905153J  DYNJ905153K  DYNJ905153L    GYNE LAPAROTOMY PACK-LF    DYNJ49593A    LAPAROSCOPY    DYNJ905157G   DYNJ905157I   DYNJ905157J     LAPAROSCOPY PACK    DYNJ56930B     MAJOR PLUS PACK    DYNJ905160J   DYNJ905160K   DYNJ905160M     MINIMALLY INVASIVE PACK-LF    DYNJ0843063K     PERCUTANEOUS TRAY    DYNJ80196     ROBOTIC PACK    DYNJ908706   DYNJ908706B]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220726</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220726</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    CATARACT FULL BODY    DYNJ85743     MAJOR VASCULAR PACK    DYNJ81610C     MINIMALLY INVASIVE PACK-LF    DYNJ0843063L     PEDIATRIC CATH ANGIO PACK    DYNJ54755J     PERIPHERAL ARTERIOGRAM RAD    DYNJ61383C     POSTERIOR SPINE PACK-LF    DYNJ0843339O     UPPER EXTREMITY    DYNJ61907A     VISCERAL ANGIOGRAM PACK-LF           DYNJ0429121L]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220742</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220742</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIO DRAPE PACK (ADLUG)642-LF    DYNJ47665D     ANGIO PACK    DYNJ30565D     ANGIOGRAPHY PACK-LF    DYNJ0854485V     ARTERIOGRAM    DYNJ28082D   DYNJ28082F     CARDIAC CATH    DYNJ67349     CARDIAC CATH PACK    DYNJ57874C     CATH I PLUS-LF    DYNJSCL100     CATH III PLUS-LF    DYNJSCL300     CATH LAB ANGIOGRAPHY PACK    DYNJ50779F     CATH LAB PACK    DYNJ41088B   DYNJ48085     CATH LAB TRAY    DYNJ37389N   DYNJ37389O     CATH PACK    DYNJ62595A   DYNJ69997     EP DRAPE PACK-LF    DYNJ47645B     HOSPITAL REGIONAL DE CONCEPCIO    DYNJ67918A     INTERVENTIONAL PACK    DYNJ56666C     INTERVENTIONAL RAD PACK    DYNJ44100L     INTERVENTIONAL RADIOLOGY PACK    DYNJ43664     INTERVENTIONAL RADIOLOGY PK-LF    DYNJ0516014AF     OR HYBRID-MRMC    DYNJ907758A     VMA TRAY    DYNJ62376A]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220750</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220750</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    CENTRAL LINE TRAY    DYNJ41089     FISTULAGRAM PACK    DYNJ62827A     FISTULOGRAM PACK    DYNJ47899A     INVASIVE LINE INSERTION    DYNJ44123B     NON VASCULAR PACK    DYNJ68037A     VASCULAR ACCESS PACK-LF    DYNJ0101291F]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220753</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220753</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes.    ANGIO PACK    DYNJ30565C   DYNJ32555B     ANGIO PACK-LF    DYNJ0774765U     ANGIO TRAY    DYNJ46153A     ANGIOGRAM TRAY    DYNJ33638K     ANGIOGRAPHY DRAPE PK QVH-LF    DYNJ35110D     ANGIOGRAPHY PACK    DYNJ44293D     ANGIOGRAPHY PACK-LF    DYNJ0854485T   DYNJ35916J     GENERAL ANGIO PACK    DYNJ57760B     GENERAL ENDO PACK-LF    DYNJ0842873J     JUDKINS PACK    DYNJ51126A     RADIOLOGY ANGIO MAJOR PACK    DYNJ62858B     TAVR JUDKINS PACK    DYNJ51127B]]></description>
				<pubDate>Fri, 26 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220743</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220743</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Neurovascular - InZone Detachment System - Class 2 Recall]]></title>
				<description><![CDATA[INZONE DETACHMENT SYSTEM, REF: M00345100950]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219266</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219266</guid>
			</item>
	
	
			<item>
				<title><![CDATA[IPG Medical Corporation - Thuvera - Class 2 Recall]]></title>
				<description><![CDATA[Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220724</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220724</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 3.0 mm, Extendable, Model/Catalog Number: 30.000.SEE.U2; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220179</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220179</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220183</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220183</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220185</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220185</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220191</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220191</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220194</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220194</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220197</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220197</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.H1; burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220192</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220192</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.070.NVG.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220184</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220184</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 40 mm, Long, Model/Catalog Number: 40.125.NVG.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220187</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220187</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.140.SHD.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220196</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220196</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220182</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220182</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 4.0 mm, Short, Model/Catalog Number: 40.125.NVG.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220186</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220186</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Long, Model/Catalog Number: 54.125.NVG.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220195</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220195</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220189</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220189</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 3.0 mm, Long, Model/Catalog Number: 30.125.NVG.U2; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220181</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220181</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Short, Model/Catalog Number: 54.070.NVG.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220190</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220190</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Medium, Model/Catalog Number: 54.085.SHD.U1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220193</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220193</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 3.0 mm, Short, Model/Catalog Number: 30.070.NVG.U2; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220180</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220180</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SURGIFY MEDICAL OY - Surgify Halo - Class 2 Recall]]></title>
				<description><![CDATA[Surgify Halo, 5.4 mm, Extendable, Model/Catalog Number: 54.000.SEE.H1; drills, burrs, trephines &amp; accessories (simple, powered)]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220188</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220188</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips North America Llc - Philips Telemetry Monitor 5500 1.4 GHz. - Class 2 Recall]]></title>
				<description><![CDATA[Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descriptions: TELE Monitor 5500, 1.4 Ghz, ECG only, ex; Telemetry Monitor 5500 1.4 GHz FAST EX.]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220889</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220889</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Zimmer, Inc. - Persona Revision - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Persona Revision  Product Name: Persona Revision&#xbf; Trabecular Metal&#xbf; Femoral Distal Augment  Model/Catalog Number: 42-5572-066-10  Software Version: N/A  Product Description: Persona Revision&#xbf; Trabecular Metal&#xbf; Femoral Distal Augment Size 9, 9+ 10mm Thicknes  Component: N/A]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220738</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220738</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Dexcom, Inc. - Dexcom G7 Continuous Glucose Monitoring System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Dexcom G7 Continuous Glucose Monitoring System  Product Name: Dexcom G7 US Retail Sensor/Transmitter 1-pack  Model/Catalog Number: STP-AT-012  Software Version: N/A  Product Description: Dexcom G7 US Retail Sensor/Transmitter 1-pack  Component: Dexcom G7 Continuous Glucose Monitoring System]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220303</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220303</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems SCS - GE Healthcare - Class 2 Recall]]></title>
				<description><![CDATA[GE Healthcare AW Server 3.2 ext.6.5; Radiological Image Processing System]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220684</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220684</guid>
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			<item>
				<title><![CDATA[Medtronic Perfusion Systems - Octopus Evolution AS Tissue Stabilizer - Class 2 Recall]]></title>
				<description><![CDATA[Octopus Evolution AS Tissue Stabilizer, Model TS2500]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220292</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220292</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Perfusion Systems - Octopus 4 - Class 2 Recall]]></title>
				<description><![CDATA[Octopus 4 Tissue Stabilizer, Model 29400]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220293</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220293</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Perfusion Systems - Octopus Evolution Tissue Stabilizer - Class 2 Recall]]></title>
				<description><![CDATA[Octopus Evolution Tissue Stabilizer, Model TS2000]]></description>
				<pubDate>Thu, 25 Jun 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220291</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220291</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Zimmer, Inc. - OffAxis Comprehensive Augmented Baseplate Instrumentation - Class 2 Recall]]></title>
				<description><![CDATA[Off-Axis Comprehensive Shoulder System, Medium, Augment, Off-Axis, Reamer Guide  Model/Catalog Number: 110040241]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:49 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220690</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220690</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Zimmer, Inc. - OffAxis Alliance Glenoid Instrumentation - Class 2 Recall]]></title>
				<description><![CDATA[Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040444]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:49 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220692</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220692</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Zimmer, Inc. - OffAxis Comprehensive Augmented Baseplate Instrumentation - Class 2 Recall]]></title>
				<description><![CDATA[Off-Axis Comprehensive Shoulder System Small, Augment, Off-Axis, Reamer Guide, Model/Catalog Number: 110040240]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:49 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220689</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220689</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Zimmer, Inc. - OffAxis Alliance Glenoid Instrumentation - Class 2 Recall]]></title>
				<description><![CDATA[Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide, Model/Catalog Number: 110040476]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:49 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220693</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220693</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Zimmer, Inc. - OffAxis Comprehensive Augmented Baseplate Instrumentation - Class 2 Recall]]></title>
				<description><![CDATA[Off-Axis Comprehensive Shoulder System, Large, Augment, Off-Axis, Reamer Guide  Model/Catalog Number: 110040242]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:49 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220691</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220691</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PFM MEDICAL INC. - MultiSnare - Class 2 Recall]]></title>
				<description><![CDATA[Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:47 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220251</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220251</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Acumed LLC - Acumed Hexalob Screw - Class 2 Recall]]></title>
				<description><![CDATA[Acumed Hexalob Screw various sizes:  REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw;  3070-27009 2.7mm x 9mm NL Hexalobe Screw;  3070-27010 2.7mm x 10mm NL Hexalobe Screw;  3070-27011 2.7mm x 11mm NL Hexalobe Screw;  3070-27012 2.7mm x 12mm NL Hexalobe Screw;  3070-27013 2.7mm x 13mm NL Hexalobe Screw;  3070-27014 2.7mm x 14mm NL Hexalobe Screw;  3070-27015 2.7mm x 15mm NL Hexalobe Screw;  3070-27016 2.7mm x 16mm NL Hexalobe Screw;  3070-27017 2.7mm x 17mm NL Hexalobe Screw;  3070-27018 2.7mm x 18mm NL Hexalobe Screw;  3076-30010 3.0mm x 10mm NL Hexalobe Screw;  3076-30012 3.0mm x 12mm NL Hexalobe Screw;  3076-30014 3.0mm x 14mm NL Hexalobe Screw]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:45 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220874</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220874</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Ventec Life Systems, Inc. - VOCSNPro - Class 2 Recall]]></title>
				<description><![CDATA[VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001]]></description>
				<pubDate>Wed, 24 Jun 2026 01:07:43 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220084</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220084</guid>
			</item>
	
	
			<item>
				<title><![CDATA[TMJ Solutions Inc - TMJ Concepts PatientFitted TMJ Reconstruction Prosthesis - Class 2 Recall]]></title>
				<description><![CDATA[TMJ Bilateral Implants, REF: CHG020]]></description>
				<pubDate>Tue, 23 Jun 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218948</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218948</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips North America Llc - Philips Avalon - Class 2 Recall]]></title>
				<description><![CDATA[Philips Avalon Fetal Monitor, FM 30 Part numberM2703A]]></description>
				<pubDate>Tue, 23 Jun 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220770</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220770</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips North America Llc - Philips Avalon - Class 2 Recall]]></title>
				<description><![CDATA[Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A]]></description>
				<pubDate>Tue, 23 Jun 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220769</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220769</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - Da Vinci SP1098 Patient Side Cart (PSC) EBrake Retainer Pin - Class 2 Recall]]></title>
				<description><![CDATA[Da Vinci ASSY, PSS, SP1098, Part Number: 380601]]></description>
				<pubDate>Tue, 23 Jun 2026 01:06:34 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219527</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219527</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Thoratec LLC - HeartMate - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: HeartMate  Product Name: HM 11V Li-ion Backup Battery, ABT  Model/Catalog Number: 106128  Software Version: N/A  Product Description: The HeartMate 11 Volt Lithium Ion Standalone Backup Battery is a component of the HeartMate 3&quot; System Controller and provides power to the System Controller. The HeartMate System Controller is an external device that manages the HeartMate Left Ventricular Assist System (LVAS), including alarms, system monitoring, and communication. It contains an internal 11V lithium-ion backup battery that provides at least 15 minutes of emergency power should the main system power source fail. The backup battery must be properly installed, charges automatically during normal use, and has a 36-month service life from date of manufacture.  Component: Yes, HeartMate 3&quot; System Controller]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220520</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220520</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Thoratec LLC - HeartMate - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: HeartMate  Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits  Model/Catalog Number: 106524US  Software Version: N/A  Product Description: The HeartMate 3&quot; Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide therapeutic benefit to those affected with advanced heart failure. In service, the LVAS assumes some or all of the workload of the left ventricle, thereby restoring the patient&apos;s systemic perfusion while palliating the underlying pathology. The LVAS features a Left Ventricular Assist Device (LVAD), a blood pump intended for long-term implantation in such patients, an extracorporeal Controller, plus all of the features, controls, attachments, interfaces, power sources, supporting equipment, labeling, and tools required to achieve the desired therapeutic benefit.  Component: No]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220518</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220518</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Thoratec LLC - HeartMate - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: HeartMate  Product Name: HeartMate 3&quot; System Controller  Model/Catalog Number: 106531US  Software Version: N/A  Product Description: The HeartMate 3&quot; System Controller acts as the central power and communication hub for the HeartMate 3 LVAS. It passes power from the Power Module, the Mobile Power Unit, Lithium-Ion Batteries, or its own integrated emergency backup supply, down to the LVAD via the Driveline. The HeartMate 3 System Controller constantly monitors system performance through communication with the implanted LVAD and Controller internal measurements and alerts the user to any alarm conditions by activating membrane panel LEDs and integrated audio annunciators. Further information on alarm conditions as well as system status can be attained by the user from the front panel LCD on the System Controller. When connected to a HeartMate Touch&quot; Communication System, the System Controller sends information regarding the System Controller and Pump Status once per second to provide additional information to the user. This link also allows the clinician to set new patient operating parameters (e.g. pump speed) and provides a link for downloading trend and/or event recorder data.  Component: Yes, HeartMate 3 Left Ventricular System (LVAS) Kits]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220519</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220519</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Merit Medical Systems, Inc. - Splashwire Hydrophilic Guide Wire - Class 2 Recall]]></title>
				<description><![CDATA[Splashwire Hydrophilic Guide Wire:  REF: MSWSTDA35150  UDI-DI codes:  00884450529645  00884450529669  00884450529690    REF: MSWSTDA35180  UDI-DI codes:  00884450529645  00884450529669    REF: MSWSTDA35260EX  UDI-DI code:  00884450529683    REF: MSWSTDA3580  UDI-DI codes:  00884450529645  00884450529690  00884450529744    REF: MSWSTDS35150  UDI-DI codes:  00884450529690  00884450529744    REF: MSWSTFA35260EX  UDI-DI code:  00884450529447    REF: MSWSTFA3580  UDI-DI code:  00884450529515    REF: MSWSTFS35150  UDI-DI code:  00884450529553    The Merit Hydrophilic Guide Wire is intended to be used in the peripheral vascular system to facilitate the placement of devices during diagnostic and interventional procedures.]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:13 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219884</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219884</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Staar Surgical AG - STAAR ICL Calculation Software Version 8.00 - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: STAAR ICL Calculation Software  Software Version: Version 8.00  Product Description: The STAAR ICL Calculation Software is designed as an aide in the calculation of the size and diopter power (with residual refraction) for physician selection of the lens. For toric ICLs, an Implantation Orientation Diagram (IOD) is also produced to provide the physician with pictorial representation of the axis of rotation and alignment.    Note: The STAAR ICL Calculation Software resides on STAAR Surgical&apos;s e-commerce website in STAAR ICL planning support (Stella), as referenced in the attached recall communication.  Component: No]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220499</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220499</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Inspire Medical Systems Inc. - Inspire Medical Systems, Inc. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Inspire Medical Systems, Inc.  Product Name: Inspire stimulation Lead  Model/Catalog Number: 4063  Product Description: The Inspire&#xbf; Stimulation Lead (Model 4063) is designed to deliver stimulation to the hypoglossal nerve for the treatment of obstructive sleep apnea. The lead features a flexible, self-sizing cuff. Electrodes in the inner surface of the cuff deliver stimulation to the nerve. The lead incorporates a standard connector for coupling to the   implantable pulse generator (IPG).  Component: N/A]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220607</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220607</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Inspire Medical Systems Inc. - Inspire Medical Systems, Inc. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Inspire Medical Systems, Inc.  Product Name: Inspire Respiratory Sensing Lead  Model/Catalog Number: 4340  Software Version: N/A  Product Description: The Inspire&#xbf; Respiratory Sensing Lead (Model 4340) is designed to detect respiratory effort. The lead features a pressure sensitive membrane that converts the mechanical energy of respiration into an electrical signal. The lead incorporates a standard connector for coupling to the implantable pulse generator (IPG).  Component: N/A]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220369</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220369</guid>
			</item>
	
	
			<item>
				<title><![CDATA[BD SWITZERLAND SARL - BD Connecta BD LuerLok 360 - Class 2 Recall]]></title>
				<description><![CDATA[BD Connecta&quot; BD Luer-Lok&quot; 360 REF 394910  UDI-DI code: 00382903949106    BD Connecta&quot; Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or extension tube. The ports can be used to sample blood or for hemodynamic monitoring. When used with IV lipid nutritional products, the stopcock device can be used for up to 24 hours.]]></description>
				<pubDate>Fri, 19 Jun 2026 01:08:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220006</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220006</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Beta Bionics, Inc. - iLet ACE Pump - Class 2 Recall]]></title>
				<description><![CDATA[iLet Bionic Pancreas, REF: BB1001]]></description>
				<pubDate>Fri, 19 Jun 2026 01:07:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218974</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218974</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) CV DRAPING/BASIN, Medline Kit Number/SKU DYNJ908483A;   2) CV DRAPING/BASIN, Medline Kit Number/SKU DYNJ908483B;   3) CV DRAPING/BASIN, Medline Kit Number/SKU DYNJ908483C;   4) CV DRAPING/BASIN 2PART PACK, Medline Kit Number/SKU DYNJ89414;   5) CVG BASIN PACK SC, Medline Kit Number/SKU DYNJ38052G;   6) T/A BASIN SET, Medline Kit Number/SKU DYNJ47941F;   7) VALVE BASIN PACK SC, Medline Kit Number/SKU DYNJ38054G.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220400</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220400</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as   BASIC GYN, CW LAP GYN, D&amp;C HYSTEROSCOPY, CW LAP GYN, DEACONESS PELVIC LAP PACK, FLOYD LAP GYN, GYN LAP PACK, GYN LAPAROSCOPY, GYN MINOR PACK, etc. (see the recall documents for a full list of affected products)]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220407</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220407</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as CH OPEN HEART, ADULT CARDIAC KIT, AHT CVOR CABG, APH EMERGENCY OPEN HEART PACK, Etc. (see recall documents for a full list of products)]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220391</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220391</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND18350]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220385</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220385</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) RETINA LAC/USC CDS, Medline Kit Number/SKU CDS983775I;   2) RETINA LAC/USC CDS, Medline Kit Number/SKU CDS983775J;   3) RETINA LAC/USC CDS, Medline Kit Number/SKU CDS983775K;   4) RETINA LAC/USC CDS, Medline Kit Number/SKU CDS983775L;   5) RETINA LAC/USC CDS, Medline Kit Number/SKU CDS983775M;   6) TONSIL PACK, Medline Kit Number/SKU DYNJ84480;   7) VITRECTOMY, Medline Kit Number/SKU DYNJVB1080;   8) VITRECTOMY, Medline Kit Number/SKU DYNJVB1080A.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220433</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220433</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 14 Fr, 1000mL, Medline Product Number/SKU (REF) URO4RR14C]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220386</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220386</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) D AND C PACK, Medline Kit Number/SKU DYNJ53973C;   2) PK CUST CV A&amp;B CABRINI CO, Medline Kit Number/SKU DYNJ60583C.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220408</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220408</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    KIT URO ROBOT CYSTECTOMY, D AND C PACK, MAD D &amp; C, VPH LITHOTOMY MINOR, TRMC- PERI GYN PACK, RICH MINOR LITHOTOMY, etc. (see recall documents for a full list of products)]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220410</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220410</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  CATH 22F ROBINSON STRL 5&apos;S PK, Medline Kit Number/SKU DYNJ0040839]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220396</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220396</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) CAROTID NEURO PACK, Medline Kit Number/SKU DYNJ44926G;   2) VP SHUNT CDS, Medline Kit Number/SKU CDS983800J;   3) VP SHUNT CDS, Medline Kit Number/SKU CDS983800K.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220404</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220404</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) CHEST EXPLORATION ECMO, Medline Kit Number/SKU DYNJ63789A;   2) CORONARY/ARTERY BYPASS TRAY, Medline Kit Number/SKU DYNJ17321G;   3) D&amp;C/CYSTO, Medline Kit Number/SKU DYNJ909989B;   4) DDD LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53214;   5) DIAGNOSTIC LAPAROSCOPY, Medline Kit Number/SKU DYNJ903390K;   6) GENERAL LAPAROSCOPY, Medline Kit Number/SKU DYNJ902700C;   7) GENERAL LAPAROSCOPY, Medline Kit Number/SKU DYNJ902700D;   8) GENERAL LAPAROSCOPY, Medline Kit Number/SKU DYNJ902700F;   9) GENERAL-CVOR MINOR, Medline Kit Number/SKU DYNJ64324A;   10) GYN LAP, Medline Kit Number/SKU DYNJT7061;   11) GYN LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53631F;   12) GYN MINOR PACK, Medline Kit Number/SKU DYNJ85910;   13) KIT UROLOGY URETHROPLASTY, Medline Kit Number/SKU DYKMBNDL117A;   14) LAP, Medline Kit Number/SKU DYNJ904585B;   15) LAP, Medline Kit Number/SKU DYNJ904585C;   16) LAP CHOLE CDS, Medline Kit Number/SKU CDS983255R;   17) LAP CHOLE CDS, Medline Kit Number/SKU CDS983255S;   18) LAP CHOLE CDS, Medline Kit Number/SKU CDS983255T;   19) LAPAROSCOPY, Medline Kit Number/SKU DYNJ89908;   20) LAPAROSCOPY, Medline Kit Number/SKU DYNJ910517;   21) LAPAROSCOPY, Medline Kit Number/SKU DYNJ910517A;   22) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ06958I;   23) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ06958J;   24) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53992C;   25) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53992D;   26) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53992F;   27) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53992G;   28) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ53992I;   29) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ67160;   30) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ84211;   31) LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJHS0235C;   32) LAPAROSCOPY PACK VICTORY, Medline Kit Number/SKU DYNJ81148;   33) LAPAROSCOPY PK, Medline Kit Number/SKU DYNJ14073B;   34) LAPAROSCOPY PK, Medline Kit Number/SKU DYNJ61404A;   35) LAPAROSCOPY PK, Medline Kit Number/SKU DYNJ61404B;   36) LAPAROSCOPY PK, Medline Kit Number/SKU DYNJ61404C;   37) LAPAROSCOPY PK, Medline Kit Number/SKU DYNJ61404D;   38) LAPAROSCOPY/GYN PACK, Medline Kit Number/SKU DYNJ0384702U;   39) PACK LAPAROSCOPY, Medline Kit Number/SKU DYNJ0553254O;   40) PROCEDURE PACK DR BILIMORI, Medline Kit Number/SKU DYNJ908046A;   41) PROCEDURE PACK DR BILIMORI, Medline Kit Number/SKU DYNJ908046B;   42) PROCEDURE PACK DR BILIMORI, Medline Kit Number/SKU DYNJ908046C;   43) PROCEDURE PACK DR BILIMORI, Medline Kit Number/SKU DYNJ908046D;   44) PROCEDURE PACK DR BILIMORI, Medline Kit Number/SKU DYNJ908046F;   45) PROLAPSE PACK, Medline Kit Number/SKU DYNJ85390;   46) RICH CYSTO, Medline Kit Number/SKU DYNJ902183I;   47) RR-PEDS CHEST BLEEDER/ECMO PK, Medline Kit Number/SKU DYNJ66263B;   48) RR-PEDS CHEST BLEEDER/ECMO PK, Medline Kit Number/SKU DYNJ66263C;   49) SMJ LAPAROSCOPY PACK, Medline Kit Number/SKU DYNJ25763J;   50) WCH GENERAL LAPAROSCOPY, Medline Kit Number/SKU DYNJ902700G.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220397</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220397</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  LAPAROSCOPY COMBINED - NO NDL, Medline Kit Number/SKU DYNJ37378A]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220388</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220388</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  TONSIL PACK CATH, Medline Kit Number/SKU DYNJ65199A]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220398</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220398</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    ADULT TRACHEOSTOMY TUBE INSERT, ASC T&amp;A, CONWAY T&amp;A SINUS, EAR PACK, etc. (see the recall documents for the full list of products)]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220395</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220395</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Urethral Catheter, Red Rubber Latex, Medline Product Number/SKU (REF), French sizes:    1. DYND13508 - 08 Fr;  2. DYND13510 - 10 Fr;  3. DYND13512 - 12 Fr;  4. DYND13514 - 14 Fr;  5. DYND13515 - 15 Fr;  6. DYND13516 - 16 Fr;  7. DYND13518 - 18 Fr;  8. DYND13520 - 20 Fr;  9. DYND13522 - 22 Fr;  10. DYND13614 - 14 Fr;  11. DYND13616 - 16 Fr.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220382</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220382</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B;   2) CARDIAC SURGERY, Medline Kit/SKU DYNJ911589A;   3) CAROTID ENDARTECOMY, Medline Kit/SKU DYNJ36211D;   4) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973;   5) CHLA ECMO / CARDIAC PACK, Medline Kit/SKU DYNJ87973A;   6) CV PART 1 AND 2, Medline Kit/SKU DYNJ908879;   7) CV PART 1 AND 2, Medline Kit/SKU DYNJ908879C;   8) FEM POP CDS, Medline Kit/SKU CDS983670K;   9) LAP BASIN TRAY, Medline Kit/SKU DYNJ50908B;   10) OPEN HEART LTX CATHETERS KIT, Medline Kit/SKU DYNJ0049032A;   11) OPEN HEART PACK, Medline Kit/SKU DYNJ80549C;   12) OPEN HEART PACK, Medline Kit/SKU DYNJ80549D;   13) RR-ADULT ECMO PACK, Medline Kit/SKU DYNJ69742B;   14) TAVR, Medline Kit/SKU DYNJ906509C.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220390</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220390</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    BILAT MICRO VASECTOMY REVERSAL, Medline Kit Number/SKU DYNJ68302]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220393</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220393</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Intermittent Latex Catheter Coude Pre-Connected to Collection Bag, 16 Fr, 1000mL, Medline Product Number/SKU (REF) URO4RR16C]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220387</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220387</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  DR FERNANDEZ, Medline kit number/SKU DYNJ68808]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220402</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220402</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  PELVIC LAP PACK, Medline Kit Number/ SKU DYNJ53820B]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220406</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220406</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) BR L&amp;D PACK, Medline Kit Number/SKU DYNJ47625B;   2) GYN VAGINAL, Medline Kit Number/SKU DYNJ912219;   3) KIT MAJ VAG SET UP, Medline Kit Number/SKU DYNJ907033B;   4) MINOR VAG PACK, Medline Kit Number/SKU DYNJ68663B;   5) OB DELIVERY PACK, Medline Kit Number/SKU DYNJ14099F;   6) OB DELIVERY PACK, Medline Kit Number/SKU DYNJ14099G;   7) OB PACK, Medline Kit Number/SKU DYNJ03387B;   8) OB PACK, Medline Kit Number/SKU DYNJ03387C;   9) OB PACK, Medline Kit Number/SKU DYNJ53543B;   10) RR-D/E PACK, Medline Kit Number/SKU DYNJ62645D;   11) RR-D/E PACK, Medline Kit Number/SKU DYNJ62645F;   12) RR-D/E PACK, Medline Kit Number/SKU DYNJ62645G;   13) VAGINAL DELIVERY PACK, Medline Kit Number/SKU DYNJ04454K;   14) VAGINAL DELIVERY PACK, Medline Kit Number/SKU DYNJ04454L;   15) VAGINAL PACK, Medline Kit Number/SKU DYNJ01830G.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220405</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220405</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Pre-connected Urethral Catheterization Tray and Bag, Red Rubber Latex, 15 Fr, Medline Product Number/SKU (REF) DYND10407]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220384</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220384</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) CRANI, Medline Kit Number/SKU DYNJ908097;   2) CRANI, Medline Kit Number/SKU DYNJ908097A;   3) CRANI, Medline Kit Number/SKU DYNJ908097B;   4) CRANI, Medline Kit Number/SKU DYNJ908097C;   5) CRANI, Medline Kit Number/SKU DYNJ908097D;   6) DR TUCKER ANT TOTAL HIP, Medline Kit Number/SKU DYNJ912029;   7) JEWISH CRANI PACK, Medline Kit Number/SKU DYNJ55637B;   8) L SCOPE PACK, Medline Kit Number/SKU DYNJ43930A;   9) LAMI PACK, Medline Kit Number/SKU DYNJ67767;   10) LAVH NEW BRAUNFELS, Medline Kit Number/SKU DYNJ61136F;   11) SOI KNEE ARTHROSCOPY, Medline Kit Number/SKU DYNJV0172Q;   12) T AND A PACK, Medline Kit Number/SKU DYNJ86229.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220434</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220434</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) KIT UROLOGY URETHROPLASTY, Medline Kit Number/SKU DYKMBNDL117C;   2) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978;   3) URETHROPLASTY, Medline Kit Number/SKU DYNJ908978F.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220399</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220399</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&amp;C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&amp;C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220409</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220409</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  NURSING KIT, Medline Kit Number/SKU EDUC1044]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220403</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220403</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Urethral Catheterization Tray, Red Rubber Latex, Medline Product Number/SKU (REF), French sizes:    1. DYNC1816, 15 Fr;   2. DYND10350, 15 Fr.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220383</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220383</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as BIOBURDEN TEST KIT, Kit Uro Robot Cystectomy, etc. (see the recall documents for a full list of products)]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220401</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220401</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:    1) BNT CV PACK, Medline Kit Number/SKU DYNJ912271;   2) CV PACK PART 1, Medline Kit Number/SKU DYNJ31204D;   3) KIT PERIPHERAL VASCULAR MMC, Medline Kit Number/SKU DYNJ905368D;   4) KIT PERIVASCULAR MMC, Medline Kit Number/SKU DYNJ905368B;   5) VP SHUNT PACK, Medline Kit Number/SKU DYNJ46530I.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220392</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220392</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE Medical Procedure Kits labeled as:  ORAL RESTORATION, Medline Kit Number/SKUDYNJ86253A]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220394</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220394</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS12-120LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220277</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220277</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220002</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220002</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219999</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219999</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-75LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220004</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220004</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS5-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220275</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220275</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS12-100LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220278</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220278</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS5-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220005</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220005</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220276</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220276</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS8-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220001</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220001</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219998</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219998</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip - Class 2 Recall]]></title>
				<description><![CDATA[ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220000</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220000</guid>
			</item>
	
	
			<item>
				<title><![CDATA[MITO RED LIGHT INC - Mito Red Light, Super Mobile - Class 2 Recall]]></title>
				<description><![CDATA[Mito Red Light, Super Mobile]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:02 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220483</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220483</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Howmedica Osteonics Corp. - TRI TS BASEPLATE SIZE 4 - Class 2 Recall]]></title>
				<description><![CDATA[TRI TS BASEPLATE SIZE 4. Part Number: 5521-B-400.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220759</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220759</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Howmedica Osteonics Corp. - TRI TS BASEPLATE SIZE 3 - Class 2 Recall]]></title>
				<description><![CDATA[TRI TS BASEPLATE SIZE 3. Part Number: 5521-B-300.]]></description>
				<pubDate>Thu, 18 Jun 2026 01:07:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220758</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220758</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Giraffe OmniBed - Class 2 Recall]]></title>
				<description><![CDATA[Giraffe OmniBed, a combination of an infant incubator and an infant warmer, All Models]]></description>
				<pubDate>Thu, 18 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220362</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220362</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Giraffe OmniBed FRU - Class 2 Recall]]></title>
				<description><![CDATA[Giraffe OmniBed Field Replaceable Unit (FRU), Model Numbers 6600-1056-400 and 6600-1461-500]]></description>
				<pubDate>Thu, 18 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220365</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220365</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Giraffe OmniBed - Class 2 Recall]]></title>
				<description><![CDATA[Giraffe OmniBed Carestations and Giraffe OmniBed Carestation CS1, a combination of an infant incubator and an infant warmer, Model Numbers 2082844-001-XXX]]></description>
				<pubDate>Thu, 18 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220363</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220363</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - PHILIPS MULTIDIAGNOST ELEVA, MULTIDIAGNOST ELEVA - Class 2 Recall]]></title>
				<description><![CDATA[Philips MultiDiagnost Eleva with the following Model Numbers:    Model # 708032 for MultiDiagnost Eleva;  Model # 708034 for MultiDiagnost Eleva with Flat Detector;  Model # 708036 for MultiDiagnost Eleva;  Model # 708037 for MultiDiagnost Eleva with Flat Detector;  Model # 708038 for MultiDiagnost Eleva with Flat Detector.]]></description>
				<pubDate>Wed, 17 Jun 2026 01:09:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221089</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221089</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - ALLURA XPER OR TABLE SERIES, ALLURACLARITY XPER FD SERIES XRAY SYSTEM, ALLURA XPER FD OR TABLE SERI - Class 2 Recall]]></title>
				<description><![CDATA[Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura Xper FD10F; Model # 722003 for Allura Xper FD10; Model # 722005 for Allura Xper FD10/10; Model # 722006 for Allura Xper FD20; Model # 722008 for Allura Xper FD20 Biplane; Model # 722010 for Allura Xper FD10; Model # 722011 for Allura Xper FD10/10; Model # 722012 for Allura Xper FD20; Model # 722013 for Allura Xper FD20 Biplane; Model # 722015 for Allura Xper FD20 OR Table; Model # 722019 for Allura Xper FD10/10 OR Table; Model # 722020 for Allura Xper FD20 Biplane OR Table; Model # 722022 for Allura Xper FD10 OR Table; Model # 722023 for Allura Xper FD20 OR Table; Model # 722025 for Allura Xper FD20 Biplane OR Table; Model # 722026 for Allura Xper FD10; Model # 722027 for Allura Xper FD10/10; Model # 722028 for Allura Xper FD20; Model # 722029 for Allura Xper FD20/10; Model #722033 for Allura Xper FD10 OR Table; Model #722035 for Allura Xper FD20 OR Table; Model #722038 for Allura Xper FD20/20; Model #722039 for Allura Xper FD20/20 OR Table; Model #722058 for Allura Xper FD20/15; Model #722059 for Allura Xper FD20/15 OR Table.]]></description>
				<pubDate>Wed, 17 Jun 2026 01:09:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221090</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=221090</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Accriva Diagnostics, Inc. - directCHECK ACTLR whole blood quality control, level 2 - Class 2 Recall]]></title>
				<description><![CDATA[directCHECK ACT-LR whole blood quality control, level 2  Model/Catalog Number: DCGLR-2]]></description>
				<pubDate>Wed, 17 Jun 2026 01:09:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220338</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220338</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AMD Medicom Inc. - Ritmed Neurological Sponges - Class 2 Recall]]></title>
				<description><![CDATA[Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995C]]></description>
				<pubDate>Wed, 17 Jun 2026 01:07:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220510</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220510</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AMD Medicom Inc. - Ritmed Nurological Sponges - Class 2 Recall]]></title>
				<description><![CDATA[Ritmed Neurological Sponges, Description/REF:   0.5x0.5in, Non-Sterile/55992C;   0.5x1.0in, Non-Sterile/55993C;   0.5x3.0in, Non-Sterile/55994C;   0.75x0.75in, Non-Sterile/55995C;   1.0x1.0in, Non-Sterile/55996C;   1.0x3.0in, Non-Sterile/55997C;   0.5x1.5in, Non-Sterile/55998C]]></description>
				<pubDate>Wed, 17 Jun 2026 01:07:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220498</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220498</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smith &amp; Nephew, Inc. - TRIGEN - Class 2 Recall]]></title>
				<description><![CDATA[TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816]]></description>
				<pubDate>Wed, 17 Jun 2026 01:07:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219265</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219265</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Steris Corporation - HarmonyAIR ASeries Surgical Lighting System - Class 2 Recall]]></title>
				<description><![CDATA[ALYON Surgical Lighting System]]></description>
				<pubDate>Tue, 16 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220124</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220124</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Steris Corporation - HarmonyAIR ASeries Surgical Lighting System - Class 2 Recall]]></title>
				<description><![CDATA[HarmonyAIR A-Series Surgical Lighting System]]></description>
				<pubDate>Tue, 16 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219749</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219749</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Steris Corporation - HarmonyAIR ASeries Surgical Lighting System - Class 2 Recall]]></title>
				<description><![CDATA[HarmonyAIR A-Series Surgical Lighting System]]></description>
				<pubDate>Tue, 16 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219748</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219748</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Navigation, Inc.-Boxborough - Medtronic Oarm O2 Imaging System - Class 2 Recall]]></title>
				<description><![CDATA[Medtronic O-arm O2 Imaging System. Model Number: BI70002000.]]></description>
				<pubDate>Tue, 16 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220683</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220683</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    C SECTION  CDS985505G    C SECTION PACK  DYNJ68260D    C-SECTION  DYNJ905094B    C-SECTION RECOVERY #2  CDS820091P]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220488</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220488</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kit:    KIT: DRESSING CHANGE PED  DYNDC3359]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220425</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220425</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    BREAST-HERNIA-PORT CDS-LF  CDS984853L]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220416</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220416</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    WT LAVH PACK  DYNJ46609F]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220436</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220436</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    BASIC EYE  DYNJ905154I    TUBAL LIGATION CDS  CDS760053K]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220439</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220439</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    ABD PACK  DYNJ81673B    BARIATRIC  DYNJ902515K    BARIATRIC +  DYNJ904119O    BARIATRIC CDS  CDS983883J    BWNBORO LAP CHOLE PACK-LF  DYNJ32836B    CCSB KARIN JWIRE LUMPECTOMY  DYNJ910459B    CHRISTUS CHILDRENS LAP CHOLE  DYNJ61165G    CUH MINOR PACK-LF  DYNJ60095B    FREE FLAP CUSTOM PACK B  DYNJ82736B    FREE NIPPLE GRAFT  DYNJ911160B    GEN MINOR  DYNJ900906L    GEN SURG LAPAROSCOPY PACK  DYNJ55248F    GEN SURG MINOR PACK  DYNJ69142F    GENERAL LAP  DYNJ61475A  DYNJT3759    GENERAL LAP PACK  DYNJ61515I  DYNJT4452    GENERAL LAP PACK-LF  DYNJ37208D    GENERAL LAPAROSCOPY  DYNJ905870G    GENERAL LAPAROSCOPY PACK  DYNJ17443T  DYNJ45263B  DYNJT4504    LAP CHOLE  DYNJ45664D  DYNJ912005    LAP CHOLE PACK  DYNJ81695B    LAP CHOLE PACK-LF  DYNJ0614113C  DYNJ0618369V    LAP CHOLE PROCEDURE-LF  CDS981184D    LAP CHOLE RFD  DYNJ906302F    LAP CHOLE SURGICOUNT  DYNJ45531G    LAP CHOLE TOTE  DYNJ908339F    LAP GASTRIC BYPASS CDS  CDS860146M    LAP GASTRIC PACK  DYNJ62065A    LAP HERNIA RFD  DYNJ906301F    LAP PACK  DYNJ38871J  DYNJ51389A    LAPAROSCOPIC  CDS920082AC    LAPAROSCOPIC PACK  DYNJ52605K    LAPAROSCOPIC PACK-LF  PHS41736G    LAPAROSCOPY PACK  DYNJT8313    LAPAROSCOPY PACK-LF  DYNJ02309D  DYNJ0551175T    LAPAROSCOPY UM RF  DYNJ902324D    LAPAROSCOPY-LF  DYNJ903241B    LAPAROTOMY PACK-LF  DYNJ21091O    LARGE ABDOMINAL PACK-LF  PHS41737D    LEX GENERAL LAPAROSCOPY  DYNJ900969K    MINOR GENERAL PACK  DYNJT3884    MINOR PACK-LF  DYNJ0105608I    MINOR PK  DYNJ61335D    MINOR PROCEDURE CDS  CDS981793G    PEDIATRIC MOSES  DYNJ58864B    PK, GEN-LAPAROSCOPY  DYNJ53837B    RMC GENERAL LAPAROSCOPIC  DYNJ907087C    ROBOTIC GENERAL  DYNJ906861D    SM-GENERAL LAP PACK-LF  DYNJ0780078W    SMJ GENERAL ABDOMINAL PACK-LF  DYNJ25765Q    UOFL HOSP GENERAL LAPAROSCOPY  DYNJ909321A]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220418</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220418</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Centurion - Class 2 Recall]]></title>
				<description><![CDATA[Centurion convenience kits:    CENTRAL LINE DRESSING SV43 FCP  DYNDC2356B    DIALYSIS CATHETER MAINTENANCE KIT  DT17570    DIALYSIS DRESSING CHANGE KIT  DT21370B    DRESSING CHANGE TRAY - GOLD  DT21115B    PORT DRESSING CHANGE KIT  DYNDC2815A]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220463</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220463</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    DISCECTOMY PACK  DYNJ86476B    EAR  DYNJ81460C  DYNJ900004J  DYNJ901779J  DYNJ902900F    EAR PACK  DYNJ81419D    ENT PACK  DYNJ40498B    HEAD &amp; NECK CDS  DYNJ901246J    JEWISH DR SEVERTSON EAR  DYNJ909252C    JEWISH HEAD&amp;NECK  DYNJ909255C    KIT HEAD AND NECK MHS  DYNJ905364B    MAJOR EAR  CDS983347S    MAJOR EAR FMOL LADY OF THE LAK  DYNJ89581    MAJOR EAR PACK  DYNJT4872    MAJOR HEAD AND NECK PACK  DYNJ38985G    MAJOR HEAD NECK PACK  DYNJ45706B    MZ EAR CDS  DYNJ905642F    PARATHYROID PACK  DYNJ81389F    PK,ENT-EAR  DYNJ43700B    SM-HEAD AND NECK PACK-LF  DYNJ0780036W    THYROID CDS  CDS983693I    TYMPANOPLASTY  CDS982720S    TYMPANOPLASTY MASTOIDECTOM  DYNJ66231B    TYMPANOPLASTY PACK-LF  DYNJ62820D    WH FACIAL HEAD AND NECK PACK  DYNJ89028A    WMC COCHLEAR IMPLANT ADD ON  DYNJ907206G]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220417</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220417</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    PORT A CATH  DYNJ906818A]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220482</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220482</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    ACL PACK  DYNJ64161C    ARTHROSCOPY PACK  DYNJ47103D  DYNJ67197G  DYNJ85197A  DYNJT4007    BASIC ACCESS PACK-LF  DYNJ36698B    BASIC BACK TRAY  DYNJ89037    BASIC PEDI PACK-LF  DYNJ0171446I  DYNJ0171446J    BASIC SPINE  DYNJ910915A    BREAST PACK  DYNJ87587A    BREAST PLASTIC PACK  DYNJ84482C    C SECTION  DYNJ49172I    CAROTID ENDARTERECTOMY PACK  DYNJ48013L    CENTRAL LINE PACK-LF  DYNJ0220136S    CERVICAL FUSION  DYNJ908135B    CERVICAL SPINE PACK  DYNJ53044G    C-SECTION  DYNJ909099F    DAVINCI PROSTATE PACK  DYNJ61711C    DEPAUL FOOT &amp; ANKLE-LF  DYNJ20010L    DIEP PACK  DYNJ64964J    DYNJ43210K  DYNJ61787F  DYNJ87065    EAR CUSTOM PACK  DYNJ82564A    ENT FREE FLAP PACK SAFETY  DYNJ54720D    EP PACEMAKER SAFETY #1  DYNJ54722F    EPCH EXTREMITY PACK  DYNJ83095B    EXTREMITY PACK  DYNJ32934F    EXTREMITY PACK-LF  DYNJ68935B    FISTULA PACK  DYNJ66502B    GENDER AFFIRMING SURGERY  DYNJ66252F    GYN LAPAROSCOPY PACK AHSC  DYNJT8381    HAND PACK WATCHMAKER-LF  DYNJ34580D    HEAD &amp; NECK PACK-LF  DYNJ0282388T  DYNJ88308    HIP SCOPE  DYNJ907120D    KNEE ARTHRO PACK  DYNJ58404F    KNEE ARTHROSCOPY PACK  DYNJ84740A    LAMI OVERHEAD PACK  DYNJ46531Q    LAMINECTOMY NEURO MPH  DYNJT5271    LAMINECTOMY PACK  DYNJ68785D    LAP APPY PACK  DYNJT6005    LAP CHOLE PACK  DYNJ82087A    LEVY PACK  DYNJ83939C    MAJOR LAP VCH  DYNJ39217P    MAJOR NEURO PACK-LF  DYNJ0578916AA    MAJOR PACK  DYNJ58528J    MINOR GEN PACK  DYNJ61661B    MINOR LAPAROTOMY PACK-LF  DYNJ0753436P    MINOR PACK  DYNJ54968B    NEURO PACK  DYNJ67628D    NEURO SHUNT PACK-LF  DYNJ0578815W    OMFS PACK  DYNJ54400C    OPEN HEART PACK  DYNJT5008    OPEN HEART-LF  DYNJ48260F    OPEN LAPAROTOMY PACK  DYNJ39247I  DYNJ39247J    PACEMAKER PACK  DYNJ31461I  DYNJ61411C    PACK,ORTHO FLIP  DYNJ65471B    PED OPEN HEART PACK  DYNJ45373G    PLASTIC PACK  DYNJ82495D    PLASTICS PK - NO SYR  DYNJ62433F    PODIATRY PACK  OP7809M    PPE BUNDLE KIT  DT13351A    PROSTATE ROBOTIC PACK  DYNJ84120C    RADIAL ART LINE INSERTION  ARTNC234    ROBOTIC GENERAL WHH  DYNJT5376    ROBOTIC PACK  DYNJ47978G    RR-SPINE PACK  DYNJ62643B    SHOULDER ARTH PACK  DYNJ58410D    SHOULDER ARTHROSCOPY PACK  DYNJ54477C  DYNJT8391    SHOULDER PACK  DYNJ61052B  DYNJT3266    SHOULDER PACK-LF  DYNJ0122428K  PHS656414I    SPINE PACK  DYNJ64949C  DYNJ83649B    SPINE SHOULDER PACK  DYNJ47104D    STERILE ACCESS KIT  DYNDA2664    TOTAL KNEE PACK  DYNJ84741B    TUBAL PACK  DYNJ68253F    UNIVERSAL PACK  DYNJ83246B    VA TAMPA GENERAL ROBOTIC PACK  DYNJT6993    W.C. MINOR LAPAROTOMY PK-LF  DYNJ0509186J    ZALE OTOLOGY CDS  CDS983181G]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220467</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220467</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    HYSTERECTOMY PACK-LF  DYNJ20485L]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220489</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220489</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kit:    IV START KIT W/HUBGUARD  DYNDV2662]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220424</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220424</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[BLOCK TRAY  DYNJRA2119A    INDWELLING NERVE BLOCK  DYNJRA1011A]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220376</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220376</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline EBSI Kit  EBSI1534]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220373</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220373</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MINOR CATH LAB PACK  DYNJ84775A    OR VASCULAR ANGIO PACK  DYNJ47269D    PORT-A-CATH  DYNJ63276G]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220377</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220377</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline CCI Nerve Block Tray  DYNJRA2742    Medline CPNB  DYNJRA2716]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220375</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220375</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    INPATIENT CENTRAL LN DRSG KIT  DYNDC3525    PICC/CVC/MIDLINE DRSG CHG KIT  DT13191A    PORT A CATH  CDS982047S    VEIN ABLATION PACK  DYNJ62889C]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220415</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220415</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kit:  (82)LABOR &amp; DELIVERY C-SECTION  DYNJ907895F]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220428</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220428</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kit:    BHS NEURO  DYNJ904900N    MEDTRX NEURO PACK  DYNJ67267B    MRI DBS PACK  DYNJ9814630O    NEURO CDS-LF  CDS983383L    NEURO PACK  DYNJ59397Q  DYNJT7315    NEURO PACK-LF  DYNJ25097I    NEURO VP SHUNT/VAGAL NERVE-RF  DYNJ21925S    PK NEURO SHUNT BUMC  DYNJT6428    RR-NEURO DBS HEAD PACK-LF  DYNJ0785736M    VP SHUNT  SYNJ10307B]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220427</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220427</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    LOOP PACK  DYNJ61460C    OPEN HEART  CDS840150Y    PACEMAKER  DYNJ56297C    PACEMAKER PK  DYNJT3454    PACEMAKER/ICD PACK  DYNJ33822L    PAD OPEN HEART  DYNJ900962O    PEDIATRIC OPEN HEART  DYNJ54238L  DYNJT6766    STAZ BASIC VASCULAR  DYNJ909794C    VASCULAR ACCESS KIT  CVI5323A    VASCULAR CDS  CDS983040M]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220378</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220378</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    20CM CVC INSERTION KIT  ECVC6805B    2L 8.5FR 16CM CVC INSERTION KIT  ECVC8055A    VANTEX PI CVC 7F, 3L, 20CM BUNDLE  ECVC6915A  ECVC6985B]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220465</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220465</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kit:    HERNIA REPAIR TOTE  DYNJ908337D]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220426</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220426</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    FEMORAL BLOCK TRAY  DYNJRA1739B]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220481</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220481</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kit:  SMSC-PELVISCOPY PACK-LF  DYNJ0161619M]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220429</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220429</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    DRIVELINE MANAGEMENT KIT  EBSI1688    PORT DRESSING CHANGE KIT  EBSI1328A]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220466</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220466</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    CMH CENTRAL LINE DRESSING CHANGE KIT  EBSI1705A    CVC/PICC/MIDLINE DRESSING CHANGE KIT  EBSI1057A    DIALYSIS DRESSING CHANGE  EBSI1498    EBSI CVC DRESSING CHANGE KIT  EBSI1585    PICC DRESSING CHANGE TRAY  EBSI1621    PORT ACCESS KIT  EBSI1837]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220464</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220464</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    DAVINCI  DYNJ905836D    DAVINCI-LF  DYNJ905293I    GENERAL ROBOTICS PACK  DYNJT8308    GYN LAP  CDS860087Q    GYN LAPAROSCOPY  DYNJ910084C    GYN LAPAROSCOPY CDS  CDS982371I    GYN LAPAROSCOPY CDS #34-RF  CDS920099S    GYN LAPAROSCOPY PACK  DYNJT3887  DYNJT6876    GYN ROBOTIC CDS  CDS984228K    GYN ROBOTICS  DYNJ911843    KIT LABOR DELIVERY TUBAL LIGAT  DYKMBNDL165C    ROBOTIC LAP CHOLE CDS  CDS985442J    ROBOTIC PACK  DYNJ84725B  DYNJ910594B    ROBOTIC SURGERY PACK  DYNJ53711B    ROBOTICS PACK  DYNJ83622C    UOFL GYN LAPAROSCOPY  DYNJ909322B    WMC ROBOTIC PACK - LF  DYNJ902583O]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220431</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220431</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    BREAST IMAGING  DYNJT5893    CHOG PLASTICS  SYNJ10306A    ENDO BREAST AUGMENTATION PACK  DYNJ68023    FACIAL PLASTIC  DYNJ909926C    JVL - MODULE PLASTIC PK  DYNJ84081B    KIT MAJOR PLASTICS MOSES  DYNJ905362C    MEM MAXILLOFACIAL PACK-LF  DYNJ0660040R    MINOR BREAST PACK  DYNJ89023A    PLASTIC MAJOR SURGERY  DYNJ902510M    PLASTIC PACK  DYNJ84766    PLASTIC PACK-LF  DYNJ0578842M    PLASTICS EXTREMITY PACK  DYNJ63803C    PLASTICS PK - NO SYR  DYNJ62433D    RR-ASC-RHINOPLASTY PACK-LF  DYNJ81772C    TRANSGENDER PACK  DYNJT7588    WH PLASTIC MAJOR PACK  DYNJ89048A]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220421</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220421</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    ADD-A-CATH ARTERIAL INSERTION  ARTNC185    PED SCHOOL AGE PICC DRSG TRAY  DYNDC3291]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220487</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220487</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    BIB AV FISTULA PACK  DYNJ58304B    CARDIAC MINOR SURGICOUNT PACK  DYNJ56573B    ENDOVASCULAR PACK  DYNJ29135N    EP DEVICE  DYNJ65916B    FULL LINE ANEURYSM CDS  CDS983672P    GEN FEM POP #14-RF  DYNJ21877W    IMPLANT PACK  DYNJ39316D    OPEN HEART MRNGSD  DYNJ58354F    PACEMAKER PACK-LF  DYNJ0618174N    PACEMAKER SETUP PACK  DYNJ35761D    PACER / CATH LAB PACK-LF  DYNJ0972604A    PACER CDS  CDS983686I    PACER PACK  DYNJ52059D    PK, EP LAB PACEMAKER  DYNJ43663A    VENOUS ACCESS PACK  DYNJ45640B]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220484</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220484</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    C-SECTION KIT  DYNJ904305J    C-SECTION PACK  DYNJ69533C]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220435</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220435</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    BASIC  DYNJ905869G    BASIC PACK  DYNJ68484B    BIB GENERAL LAPAROSCOPY PA  DYNJ58305    CHRISTUS CH PEDIATRIC BASIC  DYNJ61167G    CVC INSERTION BUNDLE  CVI3940A    DAVINCI PACK SURGICOUNT  DYNJ45544F    EPCH BASIC PACK  DYNJ83094C    GENERAL PACK  DYNJ39682B  DYNJ84882    GENERAL RFD  DYNJ906336F    GENERAL SURGERY PACK  DYNJT6003    GV MACD PACK  DYNJ46952M    IMPLANT PACK - BBI AR  DYNJ63508A    KIT THORACOSCOPY  DYNJ908872F    LVAD TRAY  DM1120A    MAJOR UROLOGY PACK-LF  DYNJ0368525M    MICRODISECT DECOMPRESS-LF  DYNJ911467    MINOR PACK  DYNJ86972    MULTI PURPOSE PACK  DYNJ58406B    OPEN HEART  DYNJ903245C    P&amp;K PACK  DYNJT5838    PACK,PEDIATRIC MAJOR  DYNJ906888F    PCNL  DYNJ904468C    PEDIATRIC MINOR RFD  DYNJ906296I    PEDIATRIC PACK  DYNJ54239K    PEDIATRIC SURGERY  DYNJ81474B    PERLMUTTER PACK  DYNJT7387    RFT ISC NOBLES MINOR PACK  DYNJ43954B    ROBOTICS FMOL LADY OF THE LAKE  DYNJ89584    ROBOTICS PACK  DYNJ83622B    SCOLI PACK NTX  DYNJ68415C    SMALL ABDOMINAL PACK-LF  PHS41749G    STIM IMPLANT TRIALS  DYNJ87790A    SUPPLEMENTAL PACK  DYNJ65244    TENEX PACK  DYNDH2190    THORACIC PACK  DYNJ56616G    THORACIC PACK SHD  DYNJ68416C    THORACOSCOPY  DYNJ9425843R    THORACOTOMY PM  DYNJ906815A    THORACOTOMY THORACOSCOPY  DYNJ902882D    TRAY,NEONATAL PICC DRSG CHANGE  DYNDC1533B    UNIVERSAL-ASC  DYNJ900071C]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220423</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220423</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    DAVINCI MAIN  DYNJ908031D]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220437</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220437</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits:    ACD  DYNJ904999J    ACDF  DYNJ907336B  DYNJ910821A    ACDF PACK  DYNJ81098C    ACL  DYNJ911996    ACL ACCESSORY PACK  DYNJ86584B    ACL- LF  DYNJ905281B    ACL PACK  DYNJ67271A    ALIF  DYNJ904848L    ANTERIOR CERVICAL  DYNJ901355J    ARTHROSCOPY  DYNJ908193B    ARTHROSCOPY PACK-LF  DYNJ42963M  DYNJ52268B    ARTHROSCOPY SHOULDER  DYNJ908684A    BACK CDS-LF  CDS983364G    BACK PACK  DYNJT4339    CDH SPINE PACK  DYNJ908828D    CERVICAL CDS  DYNJ903477J    CMC ORTHO BACK TRAY  SYNJ10272B    CRANIOTOMY  DYNJ911853    CRANIOTOMY ROOSEVELT PACK  DYNJ58358F    CUSTOM HAND PACK-LF  DYNJ0537135V    CUSTOM SPINAL PACK  DYNJT7544    DISCECTOMY PACK  DYNJ86770    DJ ORTHO SPINE  DYNJ48980M    EXTREMITY PACK-LF  DYNJT4161    FOOT PACK  DYNJ53179D    GENERAL ORTHO-ACNW  DYNJ84891    GILMORE SHOULDER SCOPE PACK  DYNJ58002    GV LUMBAR LAMINECTOMY PK  DYNJ46938L    HAND PACK  DYNJ63113B  DYNJ69662A  DYNJT5855    HAND-LF  DYNJ903263B    KIT LAMINECTOMY  DYNJ908806C    KNEE ARTHROSCOPY  DYNJ902056C  DYNJ904846I    KNEE ARTHROSCOPY-LF  DYNJ905871F    KNEE SCOPE  DYNJ906986G    LAMINECTOMY  DYNJ904847K  DYNJ909505D    LAMINECTOMY CDS  CDS983115K    LAMINECTOMY CERVICAL DISC-LF  DYNJ905286G    LAMINECTOMY NEURO PACK  DYNJ58356F    LAMINECTOMY SPINE  DYNJ904139L    LOWER EXTREMITY PACK  DYNJ63114C    LUMBAR CERVICAL PACK-LF  DYNJ0101088G    LUMBAR LAMI  DYNJ905020J    LUMBAR LAMINECTOMY  DYNJ53707    LUMBAR LAMINECTOMY PACK  DYNJT4386    MAIN/LAMINECTOMY PACK-LF  DYNJ0565499AN    NJ SPINE SPECIALIST PACK  DYNJ58706F    OHOW SPINE-BACK PACK  DYNJ910097A    ORTHO NECK CDS-LF  CDS983134C    ORTHO PACK-LF  DYNJ37202G    ORTHO SPINE  DYNJ40221G    OSC BEACH CHAIR SHOULDER-LF  DYNJ905282C    PACC PETRIE ACL ADD ON PACK-LF  DYNJ58290D    PACK,ARTHROSCOPY ASC  DYNJ65484A    PACK,POSTERIOR SPINAL FUSION  DYNJ906892B    PAD LATERAL SPINE  DYNJ902158L  DYNJ902158M    PAD POSTERIOR SPINE  DYNJ902142L    PK-SPINE  DYNJ58259A    PODIATRY PACK  DYNJ62288D    POST SPINE PACK  DYNJ20509R    POSTERIOR SPINAL FUSION  DYNJ903250B    RFT ARTHROSCOPY PACK  DYNJ43956C    RFT SHOULDER PACK-NOBLE  DYNJ36331D    SA SHOULDER #2 BORDEN  DYNJ56501A    SHOULDER  DYNJ900893M  DYNJ904184I    SHOULDER ARTHROSCOPY  DYNJ904842G    SHOULDER PACK  DYNJ83483    SHOULDER PACK-LF  DYNJ42973N    SHOULDER SCOPE PACK NTX  DYNJ68399C    SPINAL PACK  DYNJ49692G    SPINE  DYNJ910451A    SPINE PACK  DYNJ20147O  DYNJ84971  DYNJ86044A  DYNJ86308C  DYNJ88917  DYNJS3069  DYNJT4163  DYNJT8396    ST CHARLES TOTAL HIP  DYNJ909593C    TOTAL HIP  DYNJ910906D    TOTAL HIP PACK  DYNJ64156B    TOTAL JOINT  DYNJ904186G    TOTAL KNEE PACK  DYNJ60967  DYNJ61409A    WMC ORTHO SPINE WMC-LF  DYNJ902528M    XLIF  DYNJ910795B]]></description>
				<pubDate>Sat, 13 Jun 2026 01:06:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220444</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220444</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Fresh Roast Systems Inc - Class 2 Recall]]></title>
				<description><![CDATA[Fresh Roast Systems ColorTrack.  Model Name: ColorTrack. Model Number: BENCH R-100]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:42 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220847</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220847</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AVID Medical, Inc. - Halyard, Towel Six Pack - Class 2 Recall]]></title>
				<description><![CDATA[Halyard, Towel Six Pack. Kit Code: AMTS70-01.]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220513</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220513</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AVID Medical, Inc. - Halyard, Drape Pack - Class 2 Recall]]></title>
				<description><![CDATA[Halyard, Drape Pack. Kit Code: LMDP36-01.]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220514</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220514</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AVID Medical, Inc. - Halyard, Eye Bag Pack - Class 2 Recall]]></title>
				<description><![CDATA[Halyard, Eye Bag Pack. Kit Code: UIEB48-01.]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220515</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220515</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AVID Medical, Inc. - Halyard, Pain Pack - Class 2 Recall]]></title>
				<description><![CDATA[Halyard, Pain Pack. Kit Code: AMPK48-01.]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220512</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220512</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Boston Scientific Corporation - Boston Scientific Orca - Class 2 Recall]]></title>
				<description><![CDATA[Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220308</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220308</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abbott Medical - Merlin Patient Care System (PCS) software - Class 2 Recall]]></title>
				<description><![CDATA[Merlin&quot; Patient Care System (PCS) software  Merlin&quot; PCS 3650 programmer Model 3330 software]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220288</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220288</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Elekta, Inc. - MOSAIQ Oncology Information System - Class 2 Recall]]></title>
				<description><![CDATA[MOSAIQ Oncology Information System]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220340</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220340</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Fresenius Medical Care Holdings, Inc. - Bicarby Dialysate - Class 2 Recall]]></title>
				<description><![CDATA[Bicarby Dialysate; Model number: RFP-400-G;]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220088</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220088</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Boston Scientific Neuromodulation Corporation - Boston Scientific Clik X Anchor - Class 2 Recall]]></title>
				<description><![CDATA[Boston Scientific Model SC-4318, Clik X Anchor  REF: M365SC43180]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220250</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220250</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Boston Scientific Neuromodulation Corporation - Boston Scientific TCN Electrodes - Class 2 Recall]]></title>
				<description><![CDATA[Boston Scientific TCN Electrodes:  REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in);  REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in)  REF:TCN-15, TCN Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in);  REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45 mm (0.0175 in)  REF: TCN-5-3m, TCN Electrode, NITINOL, 3M CABLE, 5 cm x 0.45 mm (0.0175 in)  REF: TCN-10-3M, TCN Electrode, NITINOL, 3M CABLE, 10 cm x 0.45 mm (0.0175 in);  REF: TCN-15-3M, TCN Electrode, NITINOL, 3M CABLE, 15 cm x 0.45 mm (0.0175 in)  REF: TCN-20-3M, TCN Electrode, NITINOL, 3M CABLE, 20 cm x 0.45 mm (0.0175 in)]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:22 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220249</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220249</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Boston Scientific Neuromodulation Corporation - Boston Scientific CSK Electrodes - Class 2 Recall]]></title>
				<description><![CDATA[Boston Scientific CSK Electrodes:  REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm)  REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm);  REF: CSK-TC15, CSK Electrode, STAINLESS STEEL, 15 cm x 28 ga (0.36 mm);  REF: CSK-TC15-3M, CSK Electrode, STAINLESS STEEL, 3M Cable, 15 cm x 28 ga (0.36 mm)  REF: CSK-TC20, CSK Electrode, STAINLESS STEEL, 20 cm x 28 ga (0.36 mm)  REF: CSK-TC5,CSK Electrode, STAINLESS STEEL, 5 cm x 28 ga (0.36 mm);  REF: CSK-TC5-3M, CSK Electrode, STAINLESS STEEL, 3M Cable, 5 cm x 28 ga (0.36 mm)]]></description>
				<pubDate>Fri, 12 Jun 2026 01:06:22 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220248</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220248</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Inter-Med Llc - Advance Dental Products - Class 2 Recall]]></title>
				<description><![CDATA[Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,  Catalog number 504600-28]]></description>
				<pubDate>Thu, 11 Jun 2026 01:06:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220829</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220829</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DT MedTech, LLC - Hintermann Series H3 - Class 2 Recall]]></title>
				<description><![CDATA[Hintermann Series Talar Implant, Left, Size 2  REF 302112]]></description>
				<pubDate>Thu, 11 Jun 2026 01:06:57 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220366</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220366</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Healthcare Diagnostics, Inc. - Dimension Tacrolimus Flex reagent cartridge - Class 2 Recall]]></title>
				<description><![CDATA[Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay]]></description>
				<pubDate>Thu, 11 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220364</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220364</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medartis AG - Medartis APTUS - Class 2 Recall]]></title>
				<description><![CDATA[Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation]]></description>
				<pubDate>Wed, 10 Jun 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220268</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220268</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Sagemax Bioceramics, Inc. - NexxZr T Multi A3.5 W9816mm - Class 2 Recall]]></title>
				<description><![CDATA[NexxZr T Multi A3.5 W98-16mm, REF: 745451]]></description>
				<pubDate>Wed, 10 Jun 2026 01:06:34 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219890</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219890</guid>
			</item>
	
	
			<item>
				<title><![CDATA[The Binding Site Group, Ltd. - EXENT Analyser - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: EXENT Analyser  Product Name: EXENT Analyser  Model/Catalog Number: IE800.A  Software Version: 1.0.20  Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids used in conjunction with the EXENT assays.]]></description>
				<pubDate>Wed, 10 Jun 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219899</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219899</guid>
			</item>
	
	
			<item>
				<title><![CDATA[In2bones USA, LLC - NeoSpan SuperElastic Compression Staple w/Instruments - Class 2 Recall]]></title>
				<description><![CDATA[NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments   Catalog Number and Product Name  T50 SN010 NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments, Size 10x10x10  UDI-DI Code: 00817906020083    T50 SN012 NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments, Size 12x12x12  UDI-DI Code: 00817906020090    T50 SN020 NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments, Size 20x20x20  UDI-DI Code: 00817906020151    T50 SN110 NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments, Size 10x15x13  UDI-DI Code: 00817906020113    T50 SN115 NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments, Size 15Wx15x15  UDI-DI Code: 00817906020137    T50 SN118 NeoSpan&#xbf; SuperElastic Compression Staple w/Instruments, Size 18x14x14  UDI-DI Code: 00810021861364    Single/multiple component metallic bone fixation appliances and accessories  The In2Bones USA NeoSpan&quot; Compression Staple Implant w/instruments is indicated for hand and foot bone fragments, osteotomy fixation and joint arthrodesis.]]></description>
				<pubDate>Tue, 09 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220337</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220337</guid>
			</item>
	
	
			<item>
				<title><![CDATA[INSPIREMD Inc - CGuard Prime Carotid Stent System - Class 2 Recall]]></title>
				<description><![CDATA[CGuard&#xbf; Prime Carotid Stent System,  135cm, 10mmx40mm  Model/Catalog Number: CND1040]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220211</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220211</guid>
			</item>
	
	
			<item>
				<title><![CDATA[INSPIREMD Inc - CGuard Prime Carotid Stent System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: CGuard&#xbf; Prime Carotid Stent System, 135cm, 8mmx30mm  Model/Catalog Number: CND0830]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220206</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220206</guid>
			</item>
	
	
			<item>
				<title><![CDATA[INSPIREMD Inc - CGuard Prime Carotid Stent System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: CGuard Prime Carotid Stent System, 135cm, 9mx40mm  Model/Catalog Number: CND0940]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220209</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220209</guid>
			</item>
	
	
			<item>
				<title><![CDATA[INSPIREMD Inc - CGuard Prime Carotid Stent System - Class 2 Recall]]></title>
				<description><![CDATA[CGuard Prime Carotid Stent System,  135cm, 10mmx30mm  Model/Catalog Number: CND1030]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220210</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220210</guid>
			</item>
	
	
			<item>
				<title><![CDATA[INSPIREMD Inc - CGuard Prime Carotid Stent System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: CGuard&#xbf; Prime Carotid Stent System, 135cm, 8mmx40mm  Model/Catalog Number: CND0840]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220207</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220207</guid>
			</item>
	
	
			<item>
				<title><![CDATA[INSPIREMD Inc - CGuard Prime Carotid Stent System - Class 2 Recall]]></title>
				<description><![CDATA[CGuard Prime Carotid Stent System,  135cm, 9mx30mm  Model/Catalog Number: CND0930]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220208</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220208</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ICU Medical, Inc. - Plum Solo Precision IV Pump - Class 2 Recall]]></title>
				<description><![CDATA[Plum Solo Precision IV Pump, 40001-0401]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:02 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220055</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220055</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ICU Medical, Inc. - Plum Duo Precision IV Pump - Class 2 Recall]]></title>
				<description><![CDATA[Plum Duo Precision IV Pump, 40002-0403]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:02 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220058</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220058</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ICU Medical, Inc. - Plum Duo Infusion Pump - Class 2 Recall]]></title>
				<description><![CDATA[Plum Duo Infusion Pump, 40002-0401]]></description>
				<pubDate>Sat, 06 Jun 2026 01:07:02 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220057</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220057</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Fresenius Medical Care Holdings, Inc. - Bicarby Dialysate - Class 2 Recall]]></title>
				<description><![CDATA[Bicarby&quot; Dialysate;  Model Numbers: RFP-400-G, RFP-401-G, RFP-402-G, RFP-404-G, RFP-407-G, and RFP-456-G;]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:42 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220066</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220066</guid>
			</item>
	
	
			<item>
				<title><![CDATA[HF Acquisition Co LLC - SPORETRAQ MAILIN SPORE TESTING SERVICE, 12 TESTS - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS  Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS  Model/Catalog Number: 1023770  Software Version: N/A  Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, Chemiclave&#xbf; sterilization, Ethylene Oxide sterilization, or Dry Heat sterilization processes.  The test strip is placed in the customer s sterilizer during their sterilization cycle and upon completion the sterilized test strip along with the control strip is returned to Mesa Labs for lab testing in the return envelope. Spore test results are digitally stored in HealthFirst s OnTraq smart automation tracking and reporting system for easy and secure access to a paperless archive from any device with internet access.  Component: N/A]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219496</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219496</guid>
			</item>
	
	
			<item>
				<title><![CDATA[HF Acquisition Co LLC - SPORETRAQ MAILIN SPORE TESTING SERVICE, 52 TESTS - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS  Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS  Model/Catalog Number: 1023780  Software Version: N/A  Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, Chemiclave&#xbf; sterilization, Ethylene Oxide sterilization, or Dry Heat sterilization processes.  The test strip is placed in the customer s sterilizer during their sterilization cycle and upon completion the sterilized test strip along with the control strip is returned to Mesa Labs for lab testing in the return envelope. Spore test results are digitally stored in HealthFirst s OnTraq smart automation tracking and reporting system for easy and secure access to a paperless archive from any device with internet access.  Component: N/A]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219495</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219495</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Micromed S.p.A. - SD LTM 64 PLUS - Class 2 Recall]]></title>
				<description><![CDATA[SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, Software Version: firmware 2021.02, 2022.01 or 2022.02]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220221</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220221</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips North America Llc - DigitalDiagnost C90 - Class 2 Recall]]></title>
				<description><![CDATA[DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220247</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220247</guid>
			</item>
	
	
			<item>
				<title><![CDATA[BERLIN HEART GMBH - EXCOR Pediatric VAD system - Class 2 Recall]]></title>
				<description><![CDATA[EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219845</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219845</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Allia Moveo - Class 2 Recall]]></title>
				<description><![CDATA[Allia Moveo angiographic X-ray system]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220074</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220074</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Allia IGS Pulse - Class 2 Recall]]></title>
				<description><![CDATA[Allia IGS Pulse angiographic X-ray system]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220073</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220073</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Allia IGS 7 Pulse - Class 2 Recall]]></title>
				<description><![CDATA[Allia IGS 7 Pulse angiographic X-ray system]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220072</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220072</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Allia IGS 5 Pulse - Class 2 Recall]]></title>
				<description><![CDATA[Allia IGS 5 Pulse angiographic X-ray system]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220071</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220071</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Allia IGS 3 Pulse - Class 2 Recall]]></title>
				<description><![CDATA[Allia IGS 3 Pulse angiographic X-ray system]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220070</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220070</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mozarc Medical US LLC - Mahurkar Elite PASS Trays - Class 2 Recall]]></title>
				<description><![CDATA[Mahurkar Elite PASS Trays;  Description (Product Number/CFN):  12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221416), 12 FR x 20cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222420), 12 FR x 20cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221420), 12 FR x 24cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222424), 12 FR x 24cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221424), 12 FR x 30cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221430), 12.5 FR x 13 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233413), 12.5 FR x 16 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233416), 12.5 FR x 20 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233420), 12.5 FR x 20 cm Acute Triple Lumen Catheter with Straight Extensions, PASS Tray (8888231420), 12.5 FR x 24 cm Acute Triple Lumen Catheter with Curved Extensions, PASS Tray (8888233424), 12.5 FR x 24 cm, Acute Triple Lumen Catheter with Straight Extensions PASS Tray (8888231424), 12.5 FR x 30 cm, Triple Lumen Catheter with Straight Extensions PASS Tray (8888231430), 12.5FR x 13cm Acute Triple Lumen Catheter with Straight Extensions, PASS Tray (8888231413), 12.5FR x 16cm Acute Triple Lumen Catheter with Straight Extensions, PASS Tray (8888231416), 13.5 FR x 16 cm High Flow Acute Dual Lumen Catheter with Curved Cannula, PASS Tray (8888213416), 13.5 Fr x 16cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211416), 13.5 FR x 20 cm High Flow Acute Dual Lumen Catheter with Curved Cannula, PASS Tray (8888213420), 13.5 Fr x 20cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211420), 13.5FR x 13cm High Flow Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888212413), 13.5FR x 13cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211413), 13.5FR x 16cm High Flow Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888212416), 13.5FR x 20cm High Flow Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888212420), 13.5FR x 24cm High Flow Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888211424);  for acute hemodialysis, aphaeresis, and infusion.]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220087</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220087</guid>
			</item>
	
	
			<item>
				<title><![CDATA[D.O.R.C. Dutch Opthalmic Research Center Intl B.V. - TDC VELOCE - Class 2 Recall]]></title>
				<description><![CDATA[TDC VELOCE&quot;, 25G Two Dimensional Cutter - 20k CPM;  Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219880</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219880</guid>
			</item>
	
	
			<item>
				<title><![CDATA[D.O.R.C. Dutch Opthalmic Research Center Intl B.V. - TDC VELOCE - Class 2 Recall]]></title>
				<description><![CDATA[TDC VELOCE&quot;, 27G Two Dimensional Cutter - 20k CPM;  Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219882</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219882</guid>
			</item>
	
	
			<item>
				<title><![CDATA[D.O.R.C. Dutch Opthalmic Research Center Intl B.V. - TDC VELOCE - Class 2 Recall]]></title>
				<description><![CDATA[TDC VELOCE&quot;, 23G Two Dimensional Cutter - 20k CPM;  Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219876</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219876</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors  14 Fr  PULL  Model/Catalog Number: 8180-14]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220142</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220142</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors  24 Fr  PUSH OTW  Model/Catalog Number: 8170-24]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220141</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220141</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety PEG Kit with ENFit Connector - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: CORFLO Safety PEG Kit with ENFit Connector  Model/Catalog Number: 50-6316  Product Description: Feeding Tube Kit  Component: No]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220132</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220132</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety Peg Kit - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: CORFLO  Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-4320]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220125</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220125</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety PEG Kit with ENFit Connector - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: CORFLO* Safety PEG Kit with ENFit&#xbf; Connector  Model/Catalog Number: 50-5320]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220130</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220130</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety Pek Kit - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: CORFLO  Product Name: CORFLO Safety PEG Kit  Model/Catalog Number: 30-5320]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220126</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220126</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety PEG Kit with ENFit Connector - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: CORFLO* Safety PEG Kit with ENFit&#xbf; Connector  Model/Catalog Number: 50-4320]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220129</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220129</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors  20 Fr  PULL  Model/Catalog Number: 8180-20]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220143</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220143</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  24 Fr  PULL  Model/Catalog Number: 7180-24]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220138</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220138</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  20 Fr  PUSH OTW  Model/Catalog Number: 7170-20  Product Description: Feeding Tube Kit  Component: No]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220134</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220134</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  14 Fr  PUSH OTW  Model/Catalog Number: 7170-14  Product Description: Feeding Tube Kit]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220133</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220133</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-6316]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220128</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220128</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: CORFLO* Safety PEG Kit  Model/Catalog Number: 30-6312]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220127</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220127</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors  24 Fr  PULL  Model/Catalog Number: 8180-24]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220144</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220144</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors  14 Fr  PUSH OTW  Model/Catalog Number: 8170-14  Product Description: Feeding Tube Kit  Component: No]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220139</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220139</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  20 Fr  PULL  Model/Catalog Number: 7180-20]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220137</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220137</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  24 Fr  PUSH OTW  Model/Catalog Number: 7170-24  Product Description: Feeding Tube Kit  Component: No]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220135</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220135</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - CORFLO Safety PEG Kit with ENFit Connector - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: CORFLO* Safety PEG Kit with ENFit&#xbf; Connector  Model/Catalog Number: 50-6312]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220131</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220131</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit  14 Fr  PULL  Model/Catalog Number: 7180-14]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220136</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220136</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Avanos Medical, Inc. - MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - Class 2 Recall]]></title>
				<description><![CDATA[Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors  20 Fr  PUSH OTW  Model/Catalog Number: 8170-20]]></description>
				<pubDate>Sat, 06 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220140</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220140</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Medical Solutions USA, Inc - ARTIS pheno - Class 2 Recall]]></title>
				<description><![CDATA[ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ARTIS icono ceiling Model 11328100. ARTIS icono floor Model 11327700. interventional fluoroscopic x-ray system]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:34 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220380</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220380</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Medical Solutions USA, Inc - ARTIS pheno - Class 2 Recall]]></title>
				<description><![CDATA[ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:34 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220379</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220379</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - Da Vinci 5 - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Da Vinci 5  Product Name: ASSY,DV5 TOWER,IS5000  Model/Catalog Number: 380746  Software Version: N/A  Product Description: Preface:   This report under 21 CFR 806.10 is being submitted for the dV5 system tower, as the NIR Handheld Camera or SOCK is developed and integrated as part of the dV5 system. The affected component of the dV5 system tower is the NIR handheld camera, and is supplied by Schoelly as the manufacturer. Therefore, the product description  in this report references the NIR handheld camera system.    Product Description:   The NIR handheld camera system is compatible for use with the da Vinci&#xbf; 5 system to aid in  surgery. The components of the NIR handheld camera system include a camera control unit  and a light source, NIR handheld camera, and additional components that together, connect  to the Tower of the da Vinci 5 system. When setting up the da Vinci 5 system, the image from  the NIR handheld camera system is displayed on the Tower monitor.  Component: Yes, the SOCK is the component and integrated into the dV5 system]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219095</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219095</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SSC- Surgical Specialties Corporation - Sharpoint  2.2MM, ANGLED, DOUBLE BEVEL - Class 2 Recall]]></title>
				<description><![CDATA[Sharpoint  2.2MM, ANGLED, DOUBLE- BEVEL  Model/Catalog Number: 72-2231   Microsurgical Knife]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220158</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220158</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Grace Medical, Inc. - TITANIUM/FLUOROPLASTIC PISTON - Class 2 Recall]]></title>
				<description><![CDATA[TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L    Model/Catalog Number: 409-375      Product Description: Stapes Prosthesis]]></description>
				<pubDate>Fri, 05 Jun 2026 01:06:22 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219759</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219759</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DeRoyal Industries Inc - DeRoyal Industries Covaderm Plus, Vascular Access Dressing - Class 2 Recall]]></title>
				<description><![CDATA[DeRoyal Industries Inc.   Ref 46-406, Covaderm Plus, Vascular Access Dressing 6&quot;x6&quot; (15cmx15cm)]]></description>
				<pubDate>Thu, 04 Jun 2026 01:07:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220768</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220768</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems China Co., Ltd. - MAC 5 A4 Resting ECG Analysis System - Class 2 Recall]]></title>
				<description><![CDATA[MAC 5 A4 Resting ECG Analysis System 855001-001;  MAC 5 A5 Resting ECG Analysis System 8855002-001.  Electrocardiograph]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:57 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220178</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220178</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Windstone Medical Packaging, Inc. - AMS16835 Fluids Kit  RX - Class 2 Recall]]></title>
				<description><![CDATA[Aligned Medical AMS16835 Fluids Kit   RX]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:55 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220279</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220279</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis MedStation 4000 - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis MedStation 4000  REF: 303  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220097</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220097</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis MedStation ES Tower - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis MedStation ES Tower  REF: 352  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220102</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220102</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis MedStation ES Tower - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis MedBank Tower  REF: 1145-00  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220103</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220103</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis Mini Main - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis Mini Main  REF: 349  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220101</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220101</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis Anesthesia Station ES - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis Anesthesia Station ES  REF: 327  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220099</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220099</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis MedBank Mini - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis MedBank Mini  REF: 1147-00  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220104</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220104</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis MedStation ES - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis MedStation ES  REF: 323  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220098</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220098</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Pyxis Anesthesia Station 4000 - Class 2 Recall]]></title>
				<description><![CDATA[BD Pyxis Anesthesia Station 4000  REF: 338  Medication cabinet]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:50 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220100</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220100</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Bayer Medical Care, Inc. - MEDRAD Avanta MultiPatient Administration Tube Set - Class 2 Recall]]></title>
				<description><![CDATA[Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad&#xbf; Avanta Injection System;  Catalog number: AVA 500 MPAT (Part 2 of 2);  Affected material numbers: 87629007, 60729458, 86566648;]]></description>
				<pubDate>Thu, 04 Jun 2026 01:06:46 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220075</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220075</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Shimadzu Medical Systems - TRINIAS, BRANSIST SAFIRE, RADspeed Pro - Class 2 Recall]]></title>
				<description><![CDATA[Digital Angiography System Trinias:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST safire:UD150G-40 / D150GC-40; Digital Angiography System BRANSIST alexa:UD150G-40 / D150GC-40; Digital Radiography System RADspeed Pro: UD150B-40 / UD150V-40 / UD150L-40 / UD150L-40E/D150BC-40 / D150VC-40 / D150LC-40 / D150LC-40E/D150BC-41 / D150VC-41 / D150LC-41; Digital Radiography System RADspeed safire: UD150B-40 / D150BC-40; Radiography System RADspeed fit: N/A (Integrated in the system); X-RAY R/F SYSTEM SONIALVISION safire17:UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION safire Plus: UD150B-40 / D150BC-4;0 X-RAY R/F SYSTEM SONIALVISION safire: UD150B-40 / D150BC-40; X-RAY R/F SYSTEM SONIALVISION VERSA: UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM FLUOROspeed 300:UD150B-40 / UD150V-40 / UD150L-40/D150BC-40 / D150VC-40 / D150LC-40; X-RAY R/F SYSTEM SONIALVISION G4:D150BC-40S; X-RAY R/F SYSTEM FLUOROspeed X1:D150BC-40S]]></description>
				<pubDate>Wed, 03 Jun 2026 01:07:45 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220078</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220078</guid>
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			<item>
				<title><![CDATA[Daavlin Distributing Company - Phothera 200 - Class 2 Recall]]></title>
				<description><![CDATA[Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physician, Model Numbers 210NDT4 and 210NCL4]]></description>
				<pubDate>Wed, 03 Jun 2026 01:07:41 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219877</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219877</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Kico Knee Innovation Company - ARVIS Surgical Navigation System (Impactor VBlock Assembly and Trackers A, B, C and E) - Class 2 Recall]]></title>
				<description><![CDATA[Arvis Hip &amp; Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C]]></description>
				<pubDate>Wed, 03 Jun 2026 01:07:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220015</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220015</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Kico Knee Innovation Company - ARVIS Surgical Navigation System (VBlock Assembly and Trackers A, B, C and E) - Class 2 Recall]]></title>
				<description><![CDATA[Arvis Hip &amp; Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E]]></description>
				<pubDate>Wed, 03 Jun 2026 01:07:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220014</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220014</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 7B12/12, Model Numbers:  722067, 722225 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220333</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220333</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 5M20, Model Numbers:  722228 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220332</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220332</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 7M20, Model Numbers:  722079, 722224 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220336</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220336</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 7M12, Model Numbers:  722078, 722223 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220335</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220335</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 5M12, Model Numbers:  722227 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220331</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220331</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220328</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220328</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 3M15, Model Numbers:  722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220330</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220330</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Philips Azurion 7B20/15, Model Numbers:  722068, 722226 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220334</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220334</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Oculus Technologies of Mexico, S.A. de C.V. - PhaseOne - Class 2 Recall]]></title>
				<description><![CDATA[PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220280</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220280</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien, LP - Covidien EndoStitch - Class 2 Recall]]></title>
				<description><![CDATA[Covidien EndoStitch&quot; Polysorb Single Use Loading Unit;  Product numbers: 170053 and 170071;]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220053</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220053</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Advanced Bionics, LLC - HiResolution Bionic Ear System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: HiResolution&quot; Bionic Ear System  Product Name: HiRes Ultra 3D CI HiFocus Mid Scala  Model/Catalog Number: CI-1601-04  Software Version: N/A  Product Description: The HiResolution Bionic Ear System is a cochlear implant designed to provide useful hearing to individuals with severe-to-profound hearing loss. It consists of internal and external components. The internal components include the HiRes&quot; Ultra 3D receiver and either the HiFocus&quot; SlimJ electrode or the HiFocus&quot; Mid-Scala (MS) electrode array that are implanted surgically under the skin behind the ear. The external components include a sound processor (body-worn or ear-level), a headpiece, and a cable. The system converts sound into electrical energy that activates the auditory nerve. The auditory nerve then sends information to the brain, where it is interpreted as sound.  Component: N/A]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:22 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220176</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220176</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - CASE Cardiac Testing System - Class 2 Recall]]></title>
				<description><![CDATA[CASE v7.0 Cardiac Testing System  Model no. 3031234-001  Product Code SU3]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220231</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220231</guid>
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			<item>
				<title><![CDATA[Stryker Corporation - Neptune waste management system - Class 2 Recall]]></title>
				<description><![CDATA[Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System]]></description>
				<pubDate>Tue, 02 Jun 2026 01:06:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220096</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220096</guid>
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			<item>
				<title><![CDATA[Fresenius Kabi USA, LLC - The Large Volume Pump of the Ivenix Infusion System - Class 2 Recall]]></title>
				<description><![CDATA[The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219521</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219521</guid>
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			<item>
				<title><![CDATA[Covidien LLC - Covidien MonaTherm Esophageal Stethoscope with Temperature Sensor - Class 2 Recall]]></title>
				<description><![CDATA[Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM  REF: 90042]]></description>
				<pubDate>Sat, 30 May 2026 01:07:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220016</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220016</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien LLC - Covidien MonaTherm General Purpose Temperature Probe - Class 2 Recall]]></title>
				<description><![CDATA[Covidien Mon-a-Therm general purpose temperature probe   size: 9 Fr  REF: 90050]]></description>
				<pubDate>Sat, 30 May 2026 01:07:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220029</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220029</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien LLC - Covidien MonaTherm General Purpose Temperature Probe - Class 2 Recall]]></title>
				<description><![CDATA[Covidien Mon-a-Therm General Purpose Temperature Probe  REF: 90044]]></description>
				<pubDate>Sat, 30 May 2026 01:07:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220028</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220028</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien LLC - COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula - Class 2 Recall]]></title>
				<description><![CDATA[COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN  UDI-DI code: 60884522007028    The devices are intended for use in providing tracheal access for airway management.  Shiley Tracheostomy Tubes are double cannula tracheostomy tubes with reusable  inner cannulae (LPC, FEN, CFS, CFN, LGT) and twist-lock connectors. These Shiley  Tracheostomy Tubes have a radiopaque, biocompatible outer cannula constructed of  polyvinyl chloride.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219873</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219873</guid>
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			<item>
				<title><![CDATA[Baxter Healthcare Corporation - ExactaMix - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Exacta Mix  Product Name: Vented Micro-Volume Inlet  Model/Catalog Number: H938175     Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach the source container.]]></description>
				<pubDate>Sat, 30 May 2026 01:07:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219985</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219985</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: CESK RIVERSIDE HEALTH SYSTEM  Model/Catalog Number: 552126  Software Version: N/A  Product Description: CESK RIVERSIDE HEALTH SYSTEM  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220024</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220024</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: SESK UPMC DOUBLE CATHETER TRAY  Model/Catalog Number: 530134  Software Version: N/A  Product Description: SESK UPMC DOUBLE CATHETER TRAY  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220026</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220026</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: LYNDON B JOHNSON HOSPITAL SPINAL EPID  Model/Catalog Number: 530184  Software Version: N/A  Product Description: LYNDON B JOHNSON HOSPITAL SPINAL EPID  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220023</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220023</guid>
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			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC  Product Name: CESK NORTHSIDE ANESTHESIA TRAY  Model/Catalog Number: 555076  Software Version: N/A  Product Description: CESK NORTHSIDE ANESTHESIA TRAY  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220019</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220019</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: NES1725KFXL SPINAL EPID CLOSED TIP CATH  Model/Catalog Number: 530201  Software Version: N/A  Product Description: NES1725KFXL SPINAL EPID CLOSED TIP CATH  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220021</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220021</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: CESK HARRIS METHODIST  Model/Catalog Number: 555498  Software Version: N/A  Product Description: CESK HARRIS METHODIST  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220022</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220022</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: CESK SHANDS JACKSONVILLE 20055717  Model/Catalog Number: 555884  Software Version: N/A  Product Description: CESK SHANDS JACKSONVILLE 20055717  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220025</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220025</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. BRAUN MEDICAL INC. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: B. BRAUN MEDICAL INC.  Product Name: BPSK, BLOCKJOCKS TRAY  Model/Catalog Number: 570246  Software Version: N/A  Product Description: BPSK, BLOCKJOCKS TRAY  Component: No]]></description>
				<pubDate>Sat, 30 May 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220020</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220020</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P]]></description>
				<pubDate>Fri, 29 May 2026 01:06:44 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220034</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220034</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - GE HealthCare - Class 2 Recall]]></title>
				<description><![CDATA[GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)]]></description>
				<pubDate>Fri, 29 May 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220243</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220243</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - GE HealthCare - Class 2 Recall]]></title>
				<description><![CDATA[GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)]]></description>
				<pubDate>Fri, 29 May 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220241</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220241</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - GE HealthCare - Class 2 Recall]]></title>
				<description><![CDATA[GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)]]></description>
				<pubDate>Fri, 29 May 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220242</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220242</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - GE HealthCare - Class 2 Recall]]></title>
				<description><![CDATA[GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)]]></description>
				<pubDate>Fri, 29 May 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220245</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220245</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - GE HealthCare - Class 2 Recall]]></title>
				<description><![CDATA[GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)]]></description>
				<pubDate>Fri, 29 May 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220240</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220240</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems Information Technologies Inc - GE HealthCare - Class 2 Recall]]></title>
				<description><![CDATA[GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)]]></description>
				<pubDate>Fri, 29 May 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220244</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220244</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura - Class 2 Recall]]></title>
				<description><![CDATA[Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013), Allura Xper FD20 OR Table (722015, 722023, 722035), Allura Xper FD20 Biplane OR Table (722025), Allura Xper FD20/10 (722029), Allura Xper FD20/15 (722058), Allura Xper FD20/15 OR Table (722059), Allura Xper FD20/20 (722038), Allura Xper FD20/20 OR Table (722039);]]></description>
				<pubDate>Fri, 29 May 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219897</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219897</guid>
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			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion - Class 2 Recall]]></title>
				<description><![CDATA[Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (722079, 722224).]]></description>
				<pubDate>Fri, 29 May 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219895</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219895</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Neuromodulation - Class 2 Recall]]></title>
				<description><![CDATA[Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor]]></description>
				<pubDate>Fri, 29 May 2026 01:06:14 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220169</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220169</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Neuromodulation - Class 2 Recall]]></title>
				<description><![CDATA[Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor]]></description>
				<pubDate>Fri, 29 May 2026 01:06:14 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220167</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=220167</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Devicor Medical Products Inc - HydroMARK - Class 2 Recall]]></title>
				<description><![CDATA[HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3]]></description>
				<pubDate>Thu, 28 May 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219967</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219967</guid>
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