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			<title>Medical Device Recalls since March 25, 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>Fri, 17 Apr  2026 04:50:39 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[B Braun Medical Inc - B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG - Class 1 Recall]]></title>
				<description><![CDATA[B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219066</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219066</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT - Class 1 Recall]]></title>
				<description><![CDATA[B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219070</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219070</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT - Class 1 Recall]]></title>
				<description><![CDATA[B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219069</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219069</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA - Class 1 Recall]]></title>
				<description><![CDATA[B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219067</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219067</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC - Class 1 Recall]]></title>
				<description><![CDATA[B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long Version, FMC. Model Number: SL-2000M2095L.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219068</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219068</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B Braun Medical Inc - B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR - Class 1 Recall]]></title>
				<description><![CDATA[B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR.   Model Number: SL-2010M2096A.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219065</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219065</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Insulet Corporation - Omnipod 5 ACE Pump - Class 1 Recall]]></title>
				<description><![CDATA[Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7]]></description>
				<pubDate>Sat, 11 Apr 2026 01:06:42 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219130</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219130</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    TAVR PACK, Medline SKU # DYNJ84472]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219162</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219162</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219153</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219153</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. ROBOTIC PACK, Medline SKU # DYNJ58475F;   2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219161</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219161</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CATH LAB PACK-LF, Medline SKU 00-HCT055P;   2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q;   3. ANGIOGRAPHY CATH LAB, Medline SKU DYNJ23532C;   4. ANGIO LEFT HEART PACK, Medline SKU DYNJ40632C;   5. ANGIO DRAPE PACK, Medline SKU DYNJ47952B;   6. ANGIOGRAPHIC PACK, Medline SKU DYNJ57516;   7. CATH LAB PACK, Medline SKU DYNJ58243B;   8. CATH LAB PACK, Medline SKU DYNJ65185;   9. CSU CATH MANIFOLD KIT, Medline SKU VASC1170A;   10. MANIFOLD KIT NO TRANSDUCER, Medline SKU VASC1184A.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219149</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219149</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:  CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219147</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219147</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - NAMIC Angiographic Syringe - Class 1 Recall]]></title>
				<description><![CDATA[NAMIC Angiographic Syringe, labeled as follows:    1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027;   2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007;   3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107;   4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007;   5. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107;   6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007;   7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007;   8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107;   9. SYRINGE,12ML,W/RES,PP/FR,RA,PG, Medline SKU 70097007;   10. SYRINGE,12ML,PP/FG,RA,W/RES,-,PKG, Medline SKU 70097107;   11. SYRINGE,12ML,PP/FG,RA,W/O,RES, Medline SKU 70098107;   12. SYRINGE,20ML,TR/FR,RA,OEM,PG, Medline SKU 80075027;   13. SYRINGE,10ML,ANGIO,W/RA,-,OEM, Medline SKU 80085007;   14. SYRINGE,12ML,TR/FR,RA,OEM, Medline SKU 80087007;   15. SYRINGE,10ML,PP/FR,RA,-,OEM,-,PG, Medline SKU 80095007;   16. SYRINGE,10ML,PP/FG,RA,OEM,PG, Medline SKU 80095107;   17. SYRINGE,12ML,PP/FG,RA,-,OEM,-,PG, Medline SKU 80097107.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219145</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219145</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. SHOULDER ARTHROSCOPY PACK, Medline SKU # DYNJ30880M;    2. EXTREMITY PACK, Medline SKU # DYNJ64295A.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219197</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219197</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107; 6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007; 7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007; 8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107; 9. SYRINGE,12ML,W/RES,PP/FR,RA,PG, Medline SKU 70097007; 10. SYRINGE,12ML,PP/FG,RA,W/RES,-,PKG, Medline SKU 70097107; 11. SYRINGE,12ML,PP/FG,RA,W/O,RES, Medline SKU 70098107; 12. SYRINGE,20ML,TR/FR,RA,OEM,PG, Medline SKU 80075027; 13. SYRINGE,10ML,ANGIO,W/RA,-,OEM, Medline SKU 80085007; 14. SYRINGE,12ML,TR/FR,RA,OEM, Medline SKU 80087007; 15. SYRINGE,10ML,PP/FR,RA,-,OEM,-,PG, Medline SKU 80095007; 16. SYRINGE,10ML,PP/FG,RA,OEM,PG, Medline SKU 80095107; 17. SYRINGE,12ML,PP/FG,RA,-,OEM,-,PG, Medline SKU 80097107]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219151</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219151</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K;   2. HEART CATH PACK-LF, Medline SKU # DYNJ36478B;   3. HEART CATH PACK-LF, Medline SKU # DYNJ36478B;   4. HEART CATH PACK-LF, Medline SKU # DYNJ36478B;   5. THYROIDECTOMY, Medline SKU # DYNJ910458;   6. LH 3 PORT W/O WASTEBAG, Medline SKU # VASC1081C;   7. LHK, Medline SKU # VASC1510;   8. LHK, Medline SKU # VASC1510.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219154</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219154</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    GLOVE PACK 7.0 (15PK), Medline SKU # DYNJ63673D]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219158</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219158</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. NON VASCULAR PACK, Medline SKU # DYNJ68037C;   2. VEIN, Medline SKU # DYNJ89845;   3. VEIN, Medline SKU # DYNJ89845A.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219152</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219152</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. DELIVERY PACK, Medline SKU # DYNJ42892F;   2. DELIVERY PACK, Medline SKU # DYNJ42892G.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219160</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219160</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. ANGIO PACK, Medline SKU # DYNJ57032D;   2. NEURO INTERVENTIONAL RADIOLOGY, Medline SKU # DYNJ64026C;   3. NEURO INERVENTIONAL RADIOLOGY, Medline SKU # VASC1650.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219159</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219159</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219156</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219156</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5. MTO,SYRINGE,12ML,TR/FG,RA,W/RES, Medline SKU 70087107; 6. SYRINGE,12ML,TR/FR,RA,W/O,RES,-,PKG, Medline SKU 70088007; 7. SYRINGE,10ML,PP/FR,RA,-,PKG, Medline SKU 70095007; 8. SYRINGE,10ML,PP/FG,RA,-,PKG, Medline SKU 70095107; 9. SYRINGE,12ML,W/RES,PP/FR,RA,PG, Medline SKU 70097007; 10. SYRINGE,12ML,PP/FG,RA,W/RES,-,PKG, Medline SKU 70097107; 11. SYRINGE,12ML,PP/FG,RA,W/O,RES, Medline SKU 70098107; 12. SYRINGE,20ML,TR/FR,RA,OEM,PG, Medline SKU 80075027; 13. SYRINGE,10ML,ANGIO,W/RA,-,OEM, Medline SKU 80085007; 14. SYRINGE,12ML,TR/FR,RA,OEM, Medline SKU 80087007; 15. SYRINGE,10ML,PP/FR,RA,-,OEM,-,PG, Medline SKU 80095007; 16. SYRINGE,10ML,PP/FG,RA,OEM,PG, Medline SKU 80095107; 17. SYRINGE,12ML,PP/FG,RA,-,OEM,-,PG, Medline SKU 80097107]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219150</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219150</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. MTS RH LFT HRT KIT, Medline SKU # 60010508;   2. MTS 3V W/GUIDE, Medline SKU # 60100701;   3. ANGIOGRAPHY KIT, Medline SKU # 60131209;   4. MTS LHK, Medline SKU # 60160075;   5. MTS LHK, Medline SKU # 60161954;   6. MTO LHK, Medline SKU # 60230148;   7. GENERAL SURGERY TRAY, Medline SKU # 00-500510I;   8. BIOBURDEN TEST KIT - 686, Medline SKU # BIOB686;   9. RADIO ANGIO UNIV HOSP PACK-LF, Medline SKU # DYNJ0376145M;   10. SPECIALS PACK-LF, Medline SKU # DYNJ0392706K;   11. CARDIAC CATH PACK-LF, Medline SKU # DYNJ0451426O;   12. CARDIAC CATH PACK-LF, Medline SKU # DYNJ0451426P;   13. CARDIAC CATH PACK, Medline SKU # DYNJ07953N;   14. CATH PACK-LF, Medline SKU # DYNJ0803367J;   15. E.P. TRAY, Medline SKU # DYNJ19343J;   16. CARDIAC CATH PACK, Medline SKU # DYNJ20898T;   17. CATH LAB TRAY, Medline SKU # DYNJ24250G;   18. CATH LAB PACK-LF, Medline SKU # DYNJ38333D;   19. CATH LAB PACK-LF, Medline SKU # DYNJ38333F;   20. EP IMPLANT PACK-LF, Medline SKU # DYNJ38910D;   21. ADULT CATH LAB PACK, Medline SKU # DYNJ40380J;   22. CRANIOTOMY PACK-LF, Medline SKU # DYNJ43403D;   23. LAP CHOLE PACK, Medline SKU # DYNJ48487F;   24. CATH LAB ANGIOGRAPHY PACK, Medline SKU # DYNJ50779G;   25. CATH LAB ANGIOGRAPHY PACK, Medline SKU # DYNJ50779I;   26. HYBRID, Medline SKU # DYNJ57049N;   27. SPECIALS PK, Medline SKU # DYNJ57713C;   28. SPECIALS PK, Medline SKU # DYNJ57713D;   29. SPECIALS PK, Medline SKU # DYNJ57713F;   30. CARDIAC CATH LAB, Medline SKU # DYNJ57748A;   31. TAVR PACK, Medline SKU # DYNJ58771G;   32. CATH PACK GWV, Medline SKU # DYNJ59229F;   33. HEART CATH PACK, Medline SKU # DYNJ61294F;   34. CATH LAB PACK, Medline SKU # DYNJ61353C;   35. DEVICE IMPLANT PACK, Medline SKU # DYNJ64636A;   36. CUSTOM PROCEDURE KIT, Medline SKU # DYNJ65277A;   37. GENERAL VASCULAR PACK RFID-V2, Medline SKU # DYNJ66442F;   38. CARDIAC CATH PACK, Medline SKU # DYNJ69845C;   39. OMF MINOR PACK, Medline SKU # DYNJ83991C;   40. HEART CATH PACK, Medline SKU # DYNJ84133B;   41. SPECIAL PROCEDURES, Medline SKU # DYNJ85425B;   42. PRIMARY PACK, Medline SKU # DYNJT3093;   43. CARDIAC CATH PACK, Medline SKU # DYNJT3522A;   44. CARDIAC CATH PACK, Medline SKU # DYNJT3522B;   45. TOTAL KNEE PACK, Medline SKU # DYNJT4069;   46. CARDIAC CATH PACK, Medline SKU # DYNJT5685;   47. CATH PACK, Medline SKU # DYNJT6544;   48. PACK CARDIAC CATH, Medline SKU # DYNJT7591;   49. OBL CATH VEIN PACK, Medline SKU # DYNJT7863;   50. TUMESCENT SYRINGE KIT, Medline SKU # DYNJTUMSYR;   51. CSTM LH KIT, Medline SKU # VASC1054;   52. LHK, Medline SKU # VASC1130A;   53. MANIFOLD KIT, Medline SKU # VASC1137A;   54. LHK, Medline SKU # VASC1299A;   55. LHK, Medline SKU # VASC1399B;   56. LHK, Medline SKU # VASC1403;   57. IR 2 PORT, Medline SKU # VASC1404;   58. LHK, Medline SKU # VASC1405;   59. LHK, Medline SKU # VASC1455A;   60. TWO PORT MANIFOLD KIT, Medline SKU # VASC1496;   61. RHK, US, NAMIC MANIFOLD, Medline SKU # VASC1502;   62. LHK, Medline SKU # VASC1555;   63. 4 VALVE,PERC,MANIFOLD,KIT, Medline SKU # VASC1609;   64. LHK, Medline SKU # VASC1668;   65. LHK, Medline SKU # VASC1694;   66. LHK, Medline SKU # VASC1805;   67. TVR, Medline SKU # VASC1816.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219157</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219157</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. CSTM MANIFOLD KIT - TITUS, Medline SKU VASC1061;   2. CSTM MANIFOLD KIT - FRYE, Medline SKU VASC1074;   3. CRYO EP MANIFOLD KIT, Medline SKU VASC1198;   4. MANIFOLD KIT - 500PSI OFF, Medline SKU VASCSHPOFF1;   5. MANIFOLD KIT LOW PRESSURE ON, Medline SKU VASCSLPON1.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219148</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219148</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - NAMIC Angiographic Control Syringe - Class 1 Recall]]></title>
				<description><![CDATA[NAMIC Angiographic Control Syringe, labeled as follows:    1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007;   2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007;   3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017;   4. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007;   5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007;   6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219146</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219146</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline medical convenience kits - Class 1 Recall]]></title>
				<description><![CDATA[Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows:    1. LAPAROSCOPIC HERNIORRHAPHY DSC, Medline SKU # DYNJ63021B;   2. LAP PACK, Medline SKU # DYNJ64297B;   3. MINOR PROCEDURE PACK, Medline SKU # DYNJ82411.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219155</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219155</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy Evo O2 - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219026</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219026</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy Evo Universal - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219028</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219028</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy Evo - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219025</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219025</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy EV300 - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219027</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219027</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Baxter Healthcare Corporation - Baxter Volara - Class 1 Recall]]></title>
				<description><![CDATA[Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937.  Accessory to Baxter Volara Respiratory Therapy system.]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:34 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218810</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218810</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Abiomed Purge Cassette sold individually and within Impella Pump Sets - Class 1 Recall]]></title>
				<description><![CDATA[Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding product codes.    1. Purge Cassette, 5 Pack; Product Code: 0043-0003.     2. Impella RP US Pump Set; Product Code: 004334.     3. Purge Cassette, Packaged; Product Code: 0043-0002. Also included inside Product Code 0043-0003 above. Product Code 0043-0002 also includes innermost packaged product with Product Code 0043-0001.    4. Impella 2.5 Set; Product Code: 004413 (Customer facing code 005040).     5. Impella RP Pump Set, EU; Product Code: 0046-0011.     6. Impella CP Pump Set, EU; Product Code: 0048-0002.     7. Impella CP Pump Set BR; Product Code: 0048-0002-BR.     8. Impella CP Smart Assist Set, EU; Product Code: 0048-0014 (Also inclusive of codes 0048-0047 and 1000402 listed below).     9. Impella CP Smart Assist Set, Canada; Product Code: 0048-0044.     10. Impella CP Smart Assist Set APAC; Product Code: 0048-0047 (inclusive under code 0048-0014).    11. Impella 5.0 IMC Pump Set EU; Product Code: 005060.     12. Impella 5.5 with SmartAssist Set, EU; Product Code: 0550-0002.     13. Impella 5.5 with SmartAssist Set, CA; Product Code: 0550-0004.     14. 5.5 Accessories AU; Product Code: 1000362.     15. Impella CP Smart Assist Set; Product Code: 1000402 (inclusive under code 0048-0014).]]></description>
				<pubDate>Wed, 01 Apr 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218616</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218616</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abiomed, Inc. - Abiomed Automated Impella Controller (AIC) - Class 1 Recall]]></title>
				<description><![CDATA[Automated Impella Controller (AIC), labeled as the following with 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.     5. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU.     6. Impella Optical Controller, Packaged, UK; Product Code: 0042-0010-UK.     7. Optical AIC w/Impella Connect, Pack&apos;d, CA; Product Code: 0042-0040-CA.     8. Optical AIC w/Impella Connect, Pack&apos;d, EU; Product Code: 0042-0040-EU.     9. Optical, AIC, Impella Connect, Pkgd, AU; Product Code: 0042-0040-AU.]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218584</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218584</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Merit Medical Systems, Inc. - 16F Dual Valved Splittable Sheath Introducer - Class 1 Recall]]></title>
				<description><![CDATA[16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile), REF: FCL-174-00/B]]></description>
				<pubDate>Fri, 27 Mar 2026 01:14:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218899</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218899</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Merit Medical Systems, Inc. - CentrosFLO Hemodialysis Catheters, LongTerm Hemodialysis - Class 1 Recall]]></title>
				<description><![CDATA[CentrosFLO Hemodialysis Catheters, REF: CENFP15K/A, CENFP15K/B, CENFP17K/A, CENFP19K/A, CENFP23K/A, CENFP27K/A, CENFP31K/A, CENFT15K, CENFT15K/D, CENFT17K, CENFT17K/A, CENFT17K/D, CENFT19K, CENFT19K/A, CENFT19K/B, CENFT19K/D, CENFT23K, CENFT23K/A, CENFT23K/B, CENFT23K/D, CENFT27K, CENFT27K/A, CENFT27K/B, CENFT27K/D, CENFT31K, CENFT31K/A, CENFT31K/B, CENFT31K/D]]></description>
				<pubDate>Fri, 27 Mar 2026 01:14:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218828</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218828</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Merit Medical Systems, Inc. - Class 1 Recall]]></title>
				<description><![CDATA[ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C]]></description>
				<pubDate>Fri, 27 Mar 2026 01:14:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218898</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218898</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Merit Medical Systems, Inc. - DuraMax Chronic Hemodialysis Catheter - Class 1 Recall]]></title>
				<description><![CDATA[DuraMax Chronic Hemodialysis Catheter, REF: H787103028015/A, H787103028025/A, H787103028031/A, H787103028035/A, H787103028041/A, H787103028045/A, H787103028051/A, H787103028055/A, H787103028061/A, H787103028075/A, H787103028085/A, H787103028095/A, H787103028165/A, H787103028181/A, H787103028185/A, H787103028191/A, H787103028195/A, H787103028205/A, H787103028215/A, H787103028225/A, H787103028235/A]]></description>
				<pubDate>Fri, 27 Mar 2026 01:14:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218901</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218901</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Merit Medical Systems, Inc. - BioFlo DuraMax, Dual Valve Sheath Chronic Hemodialysis Catheter - Class 1 Recall]]></title>
				<description><![CDATA[BioFlo DuraMax Catheter, REF: H965103028011/A, H965103028021/A, H965103028021/EU, H965103028031/A, H965103028031/EU, H965103028041/A, H965103028041/EU, H965103028051/A, H965103028051/EU, H965103028061/A, H965103028061/EU, H965103028070/A, H965103028070/EU, H965103028080/A, H965103028080/EU, H965103028090/A, H965103028090/EU, H965103028161/A, H965103028181/A, H965103028191/A, H965103028191/EU, H965103028201/A, H965103028211/A, H965103028220/A, H965103028230/A, H965103028240/A, H965103038181/A]]></description>
				<pubDate>Fri, 27 Mar 2026 01:14:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218902</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218902</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy EV300 - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 27 Mar 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219022</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219022</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy Evo Universal - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 27 Mar 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219023</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219023</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy Evo - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 27 Mar 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219014</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219014</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Respironics, Inc. - Philips Respironics Trilogy Evo O2 - Class 1 Recall]]></title>
				<description><![CDATA[Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.]]></description>
				<pubDate>Fri, 27 Mar 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219019</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219019</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Navajo Manufacturing Company - Handy Solutions Heating Pad Neck and Shoulders - Class 1 Recall]]></title>
				<description><![CDATA[Handy Solutions Neck &amp; Shoulders Heating Pad, Number: 25607, Manufactured by Ninbo Unico Products Co., Ltd]]></description>
				<pubDate>Sun, 22 Mar 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218797</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218797</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Erbe USA Inc - Erbe Flexible Cryoprobe - Class 1 Recall]]></title>
				<description><![CDATA[Flexible Cryoprobe (OD 1.7mm, L1.15mm)  REF: 20402-410. For surgical use]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218709</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218709</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Erbe USA Inc - Erbe Flexible Cryoprobe - Class 1 Recall]]></title>
				<description><![CDATA[Flexible Cryoprobe (OD 1.1mm, L1.15mm) w/ oversheath (OD2.6mm, L817mm)  REF: 20402-401  STERILEEO.  For surgical use]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218707</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218707</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Erbe USA Inc - Erbe Flexible Cryoprobe - Class 1 Recall]]></title>
				<description><![CDATA[Flexible Cryoprobe (OD 2.4mm, L1.15mm)  REF: 20402-411. For surgical use]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218710</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218710</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Medical Solutions USA, Inc - ARTIS Pheno - Class 2 Recall]]></title>
				<description><![CDATA[ARTIS Pheno VE30A and VE40A, Model 10849000]]></description>
				<pubDate>Fri, 17 Apr 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219758</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219758</guid>
			</item>
	
	
			<item>
				<title><![CDATA[THERAKOS DEVELOPMENT LIMITED - Cellex Photopheresis System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Cellex Photopheresis System  Product Name: CELLEX Photopheresis Kit  Model/Catalog Number: CLXUSA  Software Version: Not Applicable  Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a  photoimmune therapy where leukocytes are separated from whole blood  via apheresis, combined with a photoactive drug (8-methoxypsoralen) and  then exposed to ultraviolet A (UVA) light. All blood components, including  the treated leukocytes, are returned to the patient.  THERAKOS&#xbf; Photopheresis utilizes the THERAKOS CELLEX System to  combine cell separation and photoactivation into a single, closed and sterile  circuit. The THERAKOS CELLEX Photopheresis System collects the buffy  coat (leukocyte-enriched blood) from the patient in a discontinuous flow  process and intermittently returns the remaining plasma and erythrocytes to  the patient. The buffy coat is passed through the photoactivation module  where the drug is activated with a precise amount of UVA light determined  by the characteristics of the individual patient s buffy coat. After  photoactivation, the buffy coat is immediately returned to the patient s  bloodstream.  Component: Not Applicable]]></description>
				<pubDate>Fri, 17 Apr 2026 01:06:24 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219081</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219081</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - CENTURION MEDICAL PRODUCTS Circumcision kit - Class 2 Recall]]></title>
				<description><![CDATA[CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F]]></description>
				<pubDate>Fri, 17 Apr 2026 01:06:22 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219261</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219261</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS - Philips Spectral CT on Rails - Class 2 Recall]]></title>
				<description><![CDATA[Philips Spectral CT on Rails. Model Number: 728334.]]></description>
				<pubDate>Fri, 17 Apr 2026 01:06:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219132</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219132</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Gentuity, LLC - Gentuity HFOCT Imaging System - Class 2 Recall]]></title>
				<description><![CDATA[Gentuity HF-OCT Imaging System Model G10-01;  Software version 23.2.13;]]></description>
				<pubDate>Fri, 17 Apr 2026 01:06:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219246</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219246</guid>
			</item>
	
	
			<item>
				<title><![CDATA[3B Medical, Inc. - React Health PHOENIX 5L Oxygen Concentrator - Class 2 Recall]]></title>
				<description><![CDATA[React Health PHOENIX 5L Oxygen Concentrator]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219086</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219086</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corp. (NeuroSciences) - Cytal Wound Matrix 2Layer 7x10 cm - Class 2 Recall]]></title>
				<description><![CDATA[Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219200</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219200</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corp. (NeuroSciences) - Cytal Wound Matrix 2Layer 5x5 cm - Class 2 Recall]]></title>
				<description><![CDATA[Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219199</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219199</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corp. (NeuroSciences) - Cytal Wound Matrix 2Layer 10x15 cm - Class 2 Recall]]></title>
				<description><![CDATA[Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219201</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219201</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corp. (NeuroSciences) - Cytal Burn Matrix 10x15 cm - Class 2 Recall]]></title>
				<description><![CDATA[Cytal Burn Matrix 10x15 cm. Product ID: BMM1015.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219203</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219203</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corp. (NeuroSciences) - Cytal Burn Matrix 7x10 cm - Class 2 Recall]]></title>
				<description><![CDATA[Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219202</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219202</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Clariance-SAS - Elegance Anterior Cervical Plate - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Elegance&#xbf; Anterior Cervical Plate  Product Name: ELEGANCE 1 LEVEL CERVICAL PLATE, ELEGANCE 2 LEVEL CERVICAL PLATE, ELEGANCE 3 LEVEL CERVICAL PLATE, ELEGANCE 4 LEVEL CERVICAL PLATE  Model/Catalog Number: See Excel sheet attached named &quot;FDA 5072 Product Information&quot;  Software Version: Not applicable Product Description: The Elegance&#xbf;Anterior Cervical plate is designed for use as a cervical plate system. It has a shape which restores the intervertebral height and lordosis. The Elegance&#xbf; Anterior Cervical plate consists in a   variety of shapes and sizes of cervical plates with rounded corners, featuring bone screw s holes, locking systems and bone screws. The plates go from one (1) to five (5) levels, and the screws are selfdrilling or self- tapping, and fixed or variable. The fixation is provided by the bone screws inserted into the vertebral body by means of an anterior approach. The Elegance&#xbf;plates, as well as the bone screws, are made of compliant ASTM F136 Titanium alloy. It is essential to insert the implants with the instrumentation specifically designed for this purpose. For more description of the instrumentation,   read the technical documentation associated to the Elegance&#xbf; Anterior Cervical plate. Detailed information concerning the surgical technique of the Elegance&#xbf;Anterior Cervical plate is available upon request, please contact CLARIANCE or its local representative.]]></description>
				<pubDate>Thu, 16 Apr 2026 01:06:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218749</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218749</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Wilson-Cook Medical Inc. - Instinct Plus Endoscopic Clipping Device - Class 2 Recall]]></title>
				<description><![CDATA[Instinct Plus Endoscopic Clipping Device  REF: G58010  Rx Only, Sterile EO]]></description>
				<pubDate>Tue, 14 Apr 2026 01:06:21 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218903</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218903</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Linkbio Corp. - LinkBio CORE Workstation, a component of the CORE Shoulder System - Class 2 Recall]]></title>
				<description><![CDATA[LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.]]></description>
				<pubDate>Sat, 11 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219141</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219141</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Philips AneurysmFlow - Class 2 Recall]]></title>
				<description><![CDATA[Philips AneurysmFlow. Model Number: 001015.     AneurysmFlow is a software medical device (Interventional Tool) intended to be used in combination with a Philips interventional X-ray system and 3DRA data.]]></description>
				<pubDate>Sat, 11 Apr 2026 01:06:37 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219103</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219103</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ARJOHUNTLEIGH POLSKA Sp. z.o.o. - Arjo Tenor Lift - Class 2 Recall]]></title>
				<description><![CDATA[Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US]]></description>
				<pubDate>Sat, 11 Apr 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219031</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219031</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Remel, Inc - YEASTONE BROTH - Class 2 Recall]]></title>
				<description><![CDATA[Yeastone Broth, 11ML, 10/BOX  YY3462]]></description>
				<pubDate>Sat, 11 Apr 2026 01:06:34 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219240</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219240</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Beta Bionics, Inc. - iLet ACE Pump, iLet Dosing Decision Software - Class 2 Recall]]></title>
				<description><![CDATA[iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software]]></description>
				<pubDate>Sat, 11 Apr 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218989</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218989</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Sustainability Solutions - Stryker Sustainability Solution Color Cuff Quick Connect Dual or Single Port Bladders - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Sustainability Solution Color Cuff 24&quot; (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235    Stryker Sustainability Solution Color Cuff 18&quot; (Red), Quick Connect Dual Port Single Bladder REF 5921-018-135    Stryker Sustainability Solution Color Cuff 18&quot; (Red) Dual Port Single Bladder REF 5921-018-235.]]></description>
				<pubDate>Fri, 10 Apr 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218944</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218944</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Beckman Coulter, Inc. - MicroScan Neg Multidrug Resistant MIC 1 - Class 2 Recall]]></title>
				<description><![CDATA[MicroScan Neg Multidrug Resistant MIC 1 REF C32368  UDI-DI code: 15099590720568    Intended Use- For use with MicroScan Dried Gram Negative  MIC/Combo Panels and Dried Gram Negative Breakpoint Combo  Panels. MicroScan panels are designed for use in determining  antimicrobial agent susceptibility and/or identification to the species level  of aerobic and facultatively anaerobic gram-negative bacilli.]]></description>
				<pubDate>Thu, 09 Apr 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219085</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219085</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Brahms GmbH - BRAHMS PlGF Plus KRYPTOR - Class 2 Recall]]></title>
				<description><![CDATA[B.R.A.H.M.S PlGF Plus KRYPTOR, Catalog Number: 859075N.  in vitro diagnostic test for Placental Growth Factor]]></description>
				<pubDate>Thu, 09 Apr 2026 01:06:33 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219084</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219084</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Medical Solutions USA, Inc - Interventional fluoroscopic xray system - Class 2 Recall]]></title>
				<description><![CDATA[ARTIS pheno and ARTIS Icono biplane, floor and ceiling. Model Numbers 10849000, 11327600, 11328100, 11327700.]]></description>
				<pubDate>Wed, 08 Apr 2026 01:08:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219414</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219414</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spacelabs Healthcare, Inc. - Spacelabs Healthcare UltraView SL Command Module - Class 2 Recall]]></title>
				<description><![CDATA[Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor]]></description>
				<pubDate>Wed, 08 Apr 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218485</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218485</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Molded Products Inc - See Luer Cap Set - Class 2 Recall]]></title>
				<description><![CDATA[See Luer Cap Set, MPC-130, set, administration, intravascular]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:22 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218833</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218833</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Wayne Pneumothorax Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Wayne Pneumothorax Tray:  Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537;   Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537;   Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537;   Reference Part Number C-UTPTY-1400-WAYNE-112497-IMH, Order Number G56537.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218937</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218937</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Approach CTO6 Micro Wire Guide - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6G, Order Number G50786]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218915</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218915</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Blue Rhino G2Multi Percutaneous Tracheostomy Introducer Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set:  Reference Part Number C-PTIS-100-HC-G-EU, Order Number G57685;   Reference Part Number C-PTIS-100-HC-G-NA, Order Number G57682;   Reference Part Number C-PTIS-100-UNL-HC-G-EU, Order Number G57687;   Reference Part Number C-PTIS-100-UNS-HC-G-EU, Order Number G57686.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218919</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218919</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - ThalQuick Chest Tube Tray - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Thal-Quick Chest Tube Tray:  Reference Part Number C-TQTSY-3200, Order Number G07242]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218932</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218932</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - NCompass Nitinol Stone Extractor - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL NCompass&#xbf; Nitinol Stone Extractor:  Reference Part Number C-NTSE-2.4-115-NC3, Order Number G36250;   Reference Part Number C-NTSE-2.4-115-NCT4, Order Number G36251.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218929</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218929</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Spectrum Central Venous Catheter Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Spectrum&#xbf; Central Venous Catheter Set:  Reference Part Number C-UDLM-401J-ABRM-HC, Order Number G43983;   Reference Part Number C-UDLM-401J-ABRM-HC-CAH, Order Number G24754;   Reference Part Number C-UDLM-401J-LSC-ABRM-HC, Order Number G43986;   Reference Part Number C-UDLM-401J-PED-ABRM-HC, Order Number G43984;   Reference Part Number C-UDLM-401J-PED-ABRM-HC-CAH, Order Number G24752;   Reference Part Number C-UDLM-401J-RSC-ABRM-HC, Order Number G43985;   Reference Part Number C-UDLM-501J-ABRM-HC, Order Number G43995;   Reference Part Number C-UDLM-501J-PED-ABRM-HC, Order Number G43996;   Reference Part Number C-UDLM-501J-RSC-ABRM-HC, Order Number G43997;   Reference Part Number C-UDLM-801J-ABRM-HC, Order Number G50817;   Reference Part Number C-UQLM-1001J-ABRM-HC-RD, Order Number G51537;   Reference Part Number C-UQLM-1001J-RSC-ABRM-HC-RD, Order Number G51539;   Reference Part Number C-UTLM-501J-ABRM-HC, Order Number G44005;   Reference Part Number C-UTLM-501J-ABRM-HC-CAH, Order Number G24803;   Reference Part Number C-UTLM-501J-LSC-ABRM-HC, Order Number G44008;   Reference Part Number C-UTLM-501J-PED-ABRM-HC, Order Number G44006;   Reference Part Number C-UTLM-501J-RSC-ABRM-HC, Order Number G44007;   Reference Part Number C-UTLM-501J-RSC-ABRM-HC-CAH, Order Number G24765;   Reference Part Number C-UTLM-701J-ABRM-HC-RD, Order Number G47825;   Reference Part Number C-UTLM-701J-ABRM-HC-RD-CAH, Order Number G24809;   Reference Part Number C-UTLM-701J-ABRM-HC-RD-P, Order Number G53599;   Reference Part Number C-UTLM-701J-LSC-ABRM-HC-RD, Order Number G47827;   Reference Part Number C-UTLM-701J-RSC-ABRM-HC-RD, Order Number G47829;   Reference Part Number C-UTLM-701J-RSC-ABRM-HC-RD-CAH, Order Number G24810.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218930</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218930</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Cook Staged Extubation Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Cook Staged Extubation Set:  Reference Part Number C-CAE-14.0-83-EXTU, Order Number G24073]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218922</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218922</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Wayne Pneumothorax Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Wayne Pneumothorax Set:  Reference Part Number C-UTPT-1020-WAYNE-IMH, Order Number G56532;   Reference Part Number C-UTPT-1400-WAYNE-112497-IMH, Order Number G56535.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218933</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218933</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Arterial Pressure Monitoring Tray - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Arterial Pressure Monitoring Tray, Reference Part Number APMY-2.5-15-0-2.5 , Order Number G58412; Reference Part Number APMY-4.0-21J-1-12, Order Number G58419]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218918</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218918</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Approach CTO12 Micro Wire Guide - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Approach CTO-12 Micro Wire Guide:   Reference Part Number CMW-14-190-12G, Order Number G50787; Reference Part Number CMW-14-300-12G, Order Number G50791]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218916</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218916</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set - Class 2 Recall]]></title>
				<description><![CDATA[Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set:  Reference Part Number C-TCCSB-500-UNI, Order Number G32193;   Reference Part Number C-TCCSB-500-UNI-01, Order Number G47665.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218925</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218925</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Approach CTO18 Micro Wire Guide - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-18G, Order Number G50788; Reference Part Number CMW-14-300-18G, Order Number G50792]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218917</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218917</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Cook Strange Bile Duct Stone Exploration Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Cook&#xbf; Strange Bile Duct Stone Exploration Set:  Reference Part Number C-CSRC-7.5D-40-STRANGE, Order Number G09108]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218924</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218924</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set:  Reference Part Number C-PTIS-100-FLEX-HC, Order Number G32092;   Reference Part Number C-PTIS-100-HC, Order Number G12115.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218921</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218921</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Blue Rhino G2Multi Percutaneous Tracheostomy Introducer Tray - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Blue Rhino&#xbf; G2-Multi Percutaneous Tracheostomy Introducer Tray:  Reference Part Number C-PTISY-100-HC-G-NA, Order Number G57703;   Reference Part Number C-PTISY-100-UNL-HC-G-NA, Order Number G57706;   Reference Part Number C-PTISY-100-UNS-HC-G-NA, Order Number G57704.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218920</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218920</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Spectrum Central Venous Tray - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Spectrum&#xbf; Central Venous Tray:  Reference Part Number C-UQLMYJ-1001J-RSC-ABRM-HC-FST-A-RD, Order Number G44800;   Reference Part Number C-UTLMYJ-701J-ABRM-HC-IHI-FST-A-RD, Order Number G44809;   Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-FST-A-RD, Order Number G44806;   Reference Part Number C-UTLMYJ-701J-RSC-ABRM-HC-IHI-FST-A-RD, Order Number G44807.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218931</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218931</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Multipurpose Drainage Catheter - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Multipurpose Drainage Catheter:  Reference Part Number ULT8.5-38-25-P-CLMS-8-RH-FS, Order Number G29775]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218928</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218928</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook Incorporated - Cook Spectrum Central Venous Catheter Tray - Class 2 Recall]]></title>
				<description><![CDATA[COOK MEDICAL Cook&#xbf; Spectrum&#xbf; Central Venous Catheter Tray:  Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0003, Order Number G56424;   Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0018, Order Number G21053;   Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0042, Order Number G34914;   Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0047, Order Number G44431;   Reference Part Number C-UTLMY-701J-ABRM-CUSTOM-0048, Order Number G44432.]]></description>
				<pubDate>Tue, 07 Apr 2026 01:06:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218923</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218923</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Tornier, Inc - Tornier HRS Max - Class 2 Recall]]></title>
				<description><![CDATA[Tornier HRS Max parts:    1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101    2. TORNIER HRS Max Tuberosity Body No Coat, Small, Cat. No. ARS1041102    3. TORNIER HRS Max Trial, Cat. No. ARS10252]]></description>
				<pubDate>Sat, 04 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218955</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218955</guid>
			</item>
	
	
			<item>
				<title><![CDATA[XTANT Medical Holdings, Inc - XTANT MEDICAL Xpress Pedicle Screw System - Class 2 Recall]]></title>
				<description><![CDATA[XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm, Part Number X073-6555-DL.]]></description>
				<pubDate>Sat, 04 Apr 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219029</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219029</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Beckman Coulter, Inc. - MicroScan Neg MIC 3J - Class 2 Recall]]></title>
				<description><![CDATA[MicroScan Neg MIC 3J REF C54814]]></description>
				<pubDate>Sat, 04 Apr 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219075</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219075</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare LLC - SIGNA Premier systems - Class 2 Recall]]></title>
				<description><![CDATA[SIGNA Premier systems]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:39 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219106</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219106</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Oxoid Australia Pty Limited - OXOID MICROBACT LISTERIA IDENTIFICATION KITS - Class 2 Recall]]></title>
				<description><![CDATA[OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219024</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219024</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 770G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 770G Insulin Pump (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219223</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219223</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 630G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218909</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218909</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 620G Insulin Pump - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 620G Insulin Pump (MMT-1750)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219228</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219228</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 530G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 530G Insulin Pump (MMT-551, MMT-751)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219453</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219453</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 640G Insulin Pump - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 640G Insulin Pump (MMT-1711, MMT-1712, MMT-1751, MMT-1752)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219224</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219224</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - Paradigm REALTime Insulin Pump - Class 2 Recall]]></title>
				<description><![CDATA[Paradigm REAL-Time Insulin Pump (MMT-522, MMT-722)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219451</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219451</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - Paradigm Insulin Pump - Class 2 Recall]]></title>
				<description><![CDATA[Paradigm Insulin Pump (MMT-712, MMT-715)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219450</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219450</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 670G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=217834</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=217834</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 720G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219226</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219226</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 780G Insulin Pump - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 780G Insulin Pump (MMT-1884, MMT-1885, MMT-1886, MMT-1894, MMT-1895, MMT-1896)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218910</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218910</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - Paradigm Veo - Class 2 Recall]]></title>
				<description><![CDATA[Paradigm REAL-Time Veo Insulin Pump (MMT-554, MMT-754)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219454</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219454</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 700G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219225</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219225</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 740G System - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed 740G Insulin Pump (MMT-1811, MMT-1812, MMT-1861, MMT-1862)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219227</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219227</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - Paradigm REALTime Revel Insulin Pump - Class 2 Recall]]></title>
				<description><![CDATA[Paradigm REAL-Time Revel Insulin Pump (MMT-523, MMT-723)]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219452</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219452</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Leg Wraps - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Leg Wraps.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218780</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218780</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Thyroid Shield - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Thyroid Shield.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218653</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218653</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Wrap Aprons - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Wrap Aprons.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218776</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218776</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Protective Sleeves - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Protective Sleeves.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218778</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218778</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Blockers - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Blockers.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218783</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218783</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218777</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218777</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Kilt Blockers - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Kilt Blockers.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218784</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218784</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical Half Aprons - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Half Aprons.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218781</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218781</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Vest - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Vest]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218773</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218773</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Frontal Aprons - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Frontal Aprons]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218775</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218775</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Caps - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Caps.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218779</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218779</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Demi Half Aprons - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Demi Half Aprons.]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218782</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218782</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Burlington Medical, LLC - Burlington Medical, Kilt - Class 2 Recall]]></title>
				<description><![CDATA[Burlington Medical, Kilt]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218774</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218774</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health 200, LLC - Monoject 1mL Luer Lock Tuberculin Syringe - Class 2 Recall]]></title>
				<description><![CDATA[Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777]]></description>
				<pubDate>Fri, 03 Apr 2026 01:06:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218994</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218994</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[THORACIC ROBOTS, DYNJ908777B]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218995</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218995</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline kits containing Olympus biopsy valves:    1. BRONCH PROCEDURE KIT, DYKE2091    2. BRONCHSCOPY, DYNJ900898G DYNJ901922I      3. BRONCHSCOPY PACK, DYNJ38313B    4. BRONCHOSCOPY PACK 0120367-LF, DYNJ32750G DYNJ32750I    5. KIT, WR THORACIC, DYNJ911252    6. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146B    7. LEX THORACIC, DYNJ902016K DYNJ902016L    8. ORGAN PROCUREMENT, DYNJ908686    9. PULMONARY PACK, DYKE1859    10. THORACIC, DYNJ901666L    11. THORACIC ROBOTICS, DYNJ908777A    12. THORACOTOMY/THORACOSCOPY, DYNJ900482N DYNJ900482O    13. XPS, DYNJ907605]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218998</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218998</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline kits containing Olympus biopsy valves:    1. BAL KIT, DYNDA2137B    2. ENDO KIT, DYKE1915]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218996</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218996</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Airway Exam Kit, DYKE1796]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218990</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218990</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[MEDLINE ANTERIOR HIP PACK  DYNJ64672B]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218999</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218999</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline kits containing Olympus biopsy valves:    1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G    2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J    3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A    4. RIGID KIT, DYNDA2138A]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218997</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218997</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Class 2 Recall]]></title>
				<description><![CDATA[Medline convenience kits containing Olympus biopsy valves:    1. BRONCH PACK, DYKE2096  2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182  3. PULMONARY BRONCH PACK, DYNDA2861A]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218991</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218991</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle Sensor  16G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle Sensor - 16G(for Aurora Trackers), Part Number 667-158]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218962</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218962</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle System Starter Kit 16G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle System Starter Kit 16G(for Aurora Trackers), Part Number 667-151]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218958</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218958</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle System Starter Kit 14G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle System Starter Kit 14G (for Aurora Trackers), Part Number 667-150]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218957</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218957</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle System Starter Kit 12G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218956</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218956</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle Sensor  18G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle Sensor - 18G (for Aurora Trackers), Part Number 667-159]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218963</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218963</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle Sensor  14G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218961</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218961</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle System Starter Kit 18G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218959</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218959</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Civco Medical Instruments Co. Inc. - eTRAX Needle Sensor  12G - Class 2 Recall]]></title>
				<description><![CDATA[eTRAX Needle Sensor - 12G (for Aurora Trackers), Part Number 667-156]]></description>
				<pubDate>Thu, 02 Apr 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218960</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218960</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - da Vinci S, Si Mega Needle Driver Instrument - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: da Vinci S, Si Mega Needle Driver Instrument  Product Name: da Vinci S, Si Mega Needle Driver Instrument  Model/Catalog Number: 420194  Software Version: NA  Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use.    All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient).  Component: NA]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218537</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218537</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - da Vinci S, Si Grasping Retractor Instrument - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: da Vinci S, Si Grasping Retractor Instrument  Product Name: da Vinci S, Si Grasping Retractor Instrument  Model/Catalog Number: 420278  Software Version: NA  Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use.    All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient).  Component: NA]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218538</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218538</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - da Vinci S, Si Monopolar Curved Scissors Instrument - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument  Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument  Model/Catalog Number: 420179  Software Version: N/A  Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use.    All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient).  Component: N/A]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218535</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218535</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - da Vinci S, Si Double Fenestrated Grasper Instrument - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument  Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument  Model/Catalog Number: 420189  Software Version: NA  Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use.    All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient).  Component: NA]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:28 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218536</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218536</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - da Vinci S, Si Permanent Cautery Hook Instrument - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument  Product Name: da Vinci S, Si Permanent Cautery Hook Instrument  Model/Catalog Number: 420183  Software Version: NA  Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use.    All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient).  Component: NA]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218633</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218633</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Intuitive Surgical, Inc. - da Vinci S, Si Tenaculum Forceps Instrument - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: da Vinci S, Si Tenaculum Forceps Instrument  Product Name: da Vinci S, Si Tenaculum Forceps Instrument  Model/Catalog Number: 420207  Software Version: N/A  Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use.    All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient).  Component: N/A]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:26 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218632</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218632</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Synthes (USA) Products LLC - 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM - Class 2 Recall]]></title>
				<description><![CDATA[2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218814</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218814</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Synthes (USA) Products LLC - 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM - Class 2 Recall]]></title>
				<description><![CDATA[2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218813</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218813</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus SOLTIVE Premium SuperPulsed Laser System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System  Product Name: SOLTIVE Premium Laser System TFL-PLS  Model/Catalog Number: TFL-PLS containing TFL-CPLU  Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tissue with moderate hemostasis, little charring, and a thin zone of necrosis.  Component: No]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218671</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218671</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus SOLTIVE Pro SuperPulsed Laser System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System  Product Name: SOLTIVE Pro Laser System TFL-SLS  Model/Catalog Number: TFL-SLS containing TFL-CSLU  Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tissue with moderate hemostasis, little charring, and a thin zone of necrosis.  Component: No]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218672</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218672</guid>
			</item>
	
	
			<item>
				<title><![CDATA[SUMMA THERAPEUTICS, LLC - Finesse BTK Multicath - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Finesse BTK Multicath  Product Name: Injectable Angioplasty Balloon Catheter  Model/Catalog Number: FS252251502  Product Description: 5 French sheath, 0.014&quot; guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon length 225mm, catheter working length 150cm  Component: NA]]></description>
				<pubDate>Tue, 31 Mar 2026 01:06:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218911</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218911</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Communications - Stryker CHROMOPHARE Softlit Ring - Class 2 Recall]]></title>
				<description><![CDATA[Stryker CHROMOPHARE Softlit Ring Surgical Light System  REF: CH00000001]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218964</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218964</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Reflexion Medical, Inc. - Class 2 Recall]]></title>
				<description><![CDATA[RefleXion X1 Radiotherapy System Model RXM1000, Part #800-00006-00]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218975</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218975</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Ultradent Products, Inc. - Jiffy - Class 2 Recall]]></title>
				<description><![CDATA[Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218657</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218657</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Waldemar Link GmbH &amp; Co. KG (Mfg Site) - LINK Embrace Shoulder System - Class 2 Recall]]></title>
				<description><![CDATA[Embrace Drill Tower, Wedged (25mm);  Item Number: 645-081/62;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:04 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218714</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218714</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Waldemar Link GmbH &amp; Co. KG (Mfg Site) - LINK Embrace Shoulder System - Class 2 Recall]]></title>
				<description><![CDATA[Embrace Drill Tower, Standard/Lateral (25mm);  Item Number: 645-081/63;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:04 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218715</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218715</guid>
			</item>
	
	
			<item>
				<title><![CDATA[BD KIESTRA LAB AUTOMATION - BD Kiestra - Class 2 Recall]]></title>
				<description><![CDATA[BD Kiestra&quot; ReadA;  Catalog No.: 446948.]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:02 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218861</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218861</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Sterile Radiology Procedure Kits - Class 2 Recall]]></title>
				<description><![CDATA[Sterile Radiology Procedure Kits, Model Number DYNDH1491B]]></description>
				<pubDate>Sat, 28 Mar 2026 01:07:00 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218988</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218988</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline Industries, LP  Puracol and Puracol Plus Collagen Wound Dressings - Class 2 Recall]]></title>
				<description><![CDATA[Puracol and Puracol Plus Collagen Wound Dressings:    MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2&quot; X 2&quot;  MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2&quot;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218891</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218891</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Healthcare Diagnostics, Inc. - Siemens Atellica CH Enzymatic Hemoglobin A1c (A1c_E) - Class 2 Recall]]></title>
				<description><![CDATA[Atellica CH Enzymatic Hemoglobin A1c (A1c_E);  Siemens Material Number (SMN): 11097536;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:57 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218934</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218934</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline ENFit Gtube Connector - Class 2 Recall]]></title>
				<description><![CDATA[ENFIT G-TUBE CONNECTOR, MEDLINE  Item No. ENFIT1010GC]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:55 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218983</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218983</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medline Industries, LP - Medline kits - Class 2 Recall]]></title>
				<description><![CDATA[Medline Kits containing ENFIT G-TUBE CONNECTOR    1. SKU DYKM2720  G/J TUBE CARE KIT    2. SKU ENFITDISCKIT  ENFIT DISCHARGE KIT]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:55 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218984</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218984</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Vue Motion V12 - Class 2 Recall]]></title>
				<description><![CDATA[Vue Motion V12. Product Number: 1017979.]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:52 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218977</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218977</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218734</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218734</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD10F; System Code: 722002;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218719</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218719</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218720</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218720</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[Allura Xper FD10C; System Code: 722001;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218718</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218718</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[Allura Xper FD20/20; System Code: 722038;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218730</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218730</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218736</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218736</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only);]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218735</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218735</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[Allura Xper FD20/15 OR Table; System Code: 722059;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218733</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218733</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218738</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218738</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218726</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218726</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218741</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218741</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 5 M12; System Code: (1)722227, (2)722231;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218742</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218742</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218721</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218721</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218740</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218740</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218724</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218724</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218725</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218725</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[Allura Xper FD20/10; System Code: 722029;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218728</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218728</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[Allura Xper FD20/20 OR Table; System Code: 722039;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218731</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218731</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[Allura Xper FD20/15; System Code: 722058;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218732</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218732</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218727</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218727</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Allura Xper - Class 2 Recall]]></title>
				<description><![CDATA[ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218723</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218723</guid>
			</item>
	
	
			<item>
				<title><![CDATA[PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - Azurion Series - Class 2 Recall]]></title>
				<description><![CDATA[Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only);]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218743</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218743</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ReCor Medical Inc. - Paradise Ultrasound Renal Denervation System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Paradise&#xbf; Ultrasound Renal Denervation System  Product Name: Paradise &#xbf; Catheter  Model/Catalog Number: PRDS-068-02  Product Description: Common name: Ablation catheter renal denervation]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218620</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218620</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ReCor Medical Inc. - Paradise Ultrasound Renal Denervation System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Paradise&#xbf; Ultrasound Renal Denervation System  Product Name: Paradise &#xbf; Catheter  Model/Catalog Number: PRDS-068-02  Product Description: Common name: Ablation catheter renal denervation]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218970</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218970</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - ARTOURA Breast Tissue Expanders - Class 2 Recall]]></title>
				<description><![CDATA[Artoura Breast Tissue Expanders  Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH  Textured, High &amp; Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218892</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218892</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - MENTOR CPX 4 US Breast Tissue Expanders with Suture Tabs - Class 2 Recall]]></title>
				<description><![CDATA[CPX 4 US Breast Tissue Expanders with Suture Tabs  Reference Numbers: SCPX-113TH, SCPX-123TH, SCPX-140TH, SCPX-146TH  Smooth Tall Height Tissue Expander, 350cc, 450cc, 650cc, 750cc]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218890</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218890</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - MENTOR CPX 4 US Breast Tissue Expanders with Suture Tabs - Class 2 Recall]]></title>
				<description><![CDATA[CPX 4 US Breast Tissue Expanders with Suture Tabs  Reference Numbers: SCPX-157LH  Smooth Low Height Tissue Expander, 650cc]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218888</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218888</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - ARTOURA Breast Tissue Expanders - Class 2 Recall]]></title>
				<description><![CDATA[Artoura Breast Tissue Expanders  Reference Numbers: SDC-100H SDC-110H SDC-120H SDC-130H SDC-135H SDC-140H SDC-150H SDC-155H  Smooth High Profile Tissue Expander, 225cc, 300cc, 375cc, 475cc, 500cc, 600cc, 750cc, 850cc]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218894</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218894</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - Mentor  CPX 4 US Breast Tissues Expanders with Suture Tabs - Class 2 Recall]]></title>
				<description><![CDATA[CPX 4 US Breast Tissue Expanders with Suture Tabs  Reference Numbers: 354-9113, 3549313, 354-9314  SILTEX Low Height Tissue Expander Style (9100, 450cc), (9300, 450cc), (9300, 550cc)]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218887</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218887</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - ARTOURA Breast Tissue Expanders - Class 2 Recall]]></title>
				<description><![CDATA[Artoura Breast Tissue Expanders  Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH  Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218895</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218895</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Mentor Texas, LP. - MENTOR CPX 4 US Breast Tissue Expanders with Suture Tabs - Class 2 Recall]]></title>
				<description><![CDATA[CPX 4 US Breast Tissue Expanders with Suture Tabs  Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH    Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc]]></description>
				<pubDate>Sat, 28 Mar 2026 01:06:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218889</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218889</guid>
			</item>
	
	
			<item>
				<title><![CDATA[CareFusion 303, Inc. - BD Alaris System with Guardrails Suite MX - Class 2 Recall]]></title>
				<description><![CDATA[BD Alaris&quot; System with Guardrails&quot; Suite MX with Point of Care Unit]]></description>
				<pubDate>Fri, 27 Mar 2026 01:06:36 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218018</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218018</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm  Product Name: Everest Bipolar Cutting Forceps  Model/Catalog Number: 3005  Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218798</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218798</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm  Product Name: Everest Bipolar Cutting Forceps  Model/Catalog Number: 3006  Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218799</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218799</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus PKS Cutting Forceps w/Cord, 5mm 24cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm  Product Name: PKS Cutting Forceps  Model/Catalog Number: 920000PK  Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using   electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218803</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218803</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus PKS Cutting Forceps, 5mm 33cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm  Product Name: PKS Cutting Forceps  Model/Catalog Number: 3005PK  Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using   electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218802</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218802</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus PK Cutting Forceps, 5mm 33cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus PK Cutting Forceps, 5mm 33cm  Product Name: PK Cutting Forceps  Model/Catalog Number: PK-CF0533  Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation during an endoscopic or open surgical procedure.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218800</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218800</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus PKS Cutting Forceps, 5mm 33cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm  Product Name: PKS Cutting Forceps  Model/Catalog Number: 920005PK  Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using   electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218804</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218804</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus HALO PKS Cutting Forceps, 5mm 33cm - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm  Product Name: HALO PKS Cutting Forceps  Model/Catalog Number: HACF0533  Product Description: The HALO PKS Cutting Forceps are intended to be passed through a 5 mm laparoscopic cannula. Coagulation   is achieved using electrosurgical energy under laparoscopic visualization. The device is intended to be used with the Gyrus ACMI G400 Workstation only.]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:30 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218801</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218801</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Tandem Diabetes Care, Inc. - t:slim X2 insulin pump with interoperable technology - Class 2 Recall]]></title>
				<description><![CDATA[Tandem pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanism to deliver insulin from within a disposable cartridge, through an infusion set, into a patient s subcutaneous tissue. As with current insulin infusion pumps on the U.S. market, the desired timing and quantity of the insulin delivery is programmed by the user (i.e., the patient).]]></description>
				<pubDate>Thu, 26 Mar 2026 01:06:29 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218867</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218867</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Straumann USA LLC - Straumann Custom Abutments - Class 2 Recall]]></title>
				<description><![CDATA[Custom Abutment AS Ti, for Straumann RC, incl. TAN screw;  Catalog Number/Art.: 010.5438;]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219093</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219093</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Straumann USA LLC - P.004 RC CARES TITANIUM AND CERAMIC ABUTMENTS - Class 2 Recall]]></title>
				<description><![CDATA[Custom Abutment Ti, for Straumann RC, incl. TAN screw;  Catalog Number/Art.: 027.4620;]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:59 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219092</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219092</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic MiniMed, Inc. - MiniMed 780G - Class 2 Recall]]></title>
				<description><![CDATA[MiniMed&quot; 780G - MMT-1884  MiniMed&quot; 780G - MMT-1886    With Software 6.60 and 6.61]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:42 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218770</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218770</guid>
			</item>
	
	
			<item>
				<title><![CDATA[AMO Puerto Rico Manufacturing, Inc. - TECNIS Eyhance IOL with TECNIS Simplicity Delivery System - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity&quot; Delivery System  Product Name: TECNIS Eyhance IOL with TECNIS Simplicity&quot; Delivery System  Model/Catalog Number: DIB00  Software Version: N/A  Product Description: The TECNIS SIMPLICITY&quot; Delivery System is designed to provide a sterile,controlled and touch-free method of delivering the lens into the eye. The lens is preloaded and pre-assembled in the delivery system. The TECNIS SIMPLICITY&quot; Delivery System Model DIB00 contains the TECNISEyhance&quot; IOL, which is a one-piece, foldable, posterior chamber lens with an overall diameter of 13.0 mm and an optic diameter of 6.0 mm. The TECNIS SIMPLICITY&quot; Delivery System is designed to provide a sterile,controlled and touch-free method of delivering the lens into the eye.  Component: No]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:40 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218617</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218617</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Orthalign, Inc - Ortho Dev. Trimax  Pegged, PREF Size 1 5 - Class 2 Recall]]></title>
				<description><![CDATA[Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 1 -5  REF:402566  component Lantern Knee System]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218966</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218966</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Orthalign, Inc - Ortho Dev. Trimax  Pegged, PREF Size 67 - Class 2 Recall]]></title>
				<description><![CDATA[Drill Plate, Ortho Dev. Trimax - Pegged, PREF Size 6-7  REF:402567  component Lantern Knee System]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:38 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218967</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218967</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Koven Technology, Inc. - BiDop 3 - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: BiDop 3  Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe  Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe).  Software Version: N/A  Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector with LCD numeric display, used with interchangeable probes to detect vascular blood-flow signals and display heart rate; affected units were packaged with a 2 MHz BT2M20S8C fetal probe and labeled for both vascular and fetal applications.]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:32 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219078</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219078</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Beckman Coulter, Inc. - MicroScan Neg MIC 56 - Class 2 Recall]]></title>
				<description><![CDATA[MicroScan Neg MIC 56 REF C42464  UDI-DI code: 15099590731212    MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:07:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219076</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=219076</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus Endoscope Air/Water Valve  MAJ1444 - Class 2 Recall]]></title>
				<description><![CDATA[Olympus Endoscope Air/Water Valve - MAJ-1444. Model Number: MAJ-1444.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218480</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218480</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus Endoscope Suction Valve  MAJ1443 - Class 2 Recall]]></title>
				<description><![CDATA[Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218479</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218479</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus Endoscope Reprocessor OERElite - Class 2 Recall]]></title>
				<description><![CDATA[Olympus Endoscope Reprocessor OER-Elite. Model Number: N5789340.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218481</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218481</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus Corporation of the Americas - Olympus Endoscope Reprocessor OERPro - Class 2 Recall]]></title>
				<description><![CDATA[Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:07:03 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218482</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218482</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Medical Systems, LLC - Imactis CTNavigation System - Class 2 Recall]]></title>
				<description><![CDATA[Imactis CT-Navigation System, stereotaxic accessory for Computer Tomography (CT), systems, Model Numbers E85101LA and E85101LP]]></description>
				<pubDate>Sat, 21 Mar 2026 01:07:01 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218785</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218785</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - HLS  Hand Locking Plates System - Class 2 Recall]]></title>
				<description><![CDATA[HLS - Hand Locking Plates System with the below descriptions and corresponding article numbers.     1. Cortical Screw; Article Numbers: 32151-6, 32151-8, 32151-9, 32151-10, 32151-11, 32151-12, 32151-13, 32151-14, 32151-15, 32151-16, 32151-18, 32151-20.     2. HLS Plate, 2 T-Shape; Article Numbers: 21505-4, 21506-4.     3. HLS Plate, 3 T-Shape; Article Numbers: 21507-4, 21508-4.     4. HLS Plate, Square; Article Numbers: 21517.     5. HLS Plate, Straight; Article Numbers: 21502, 21503-4, 21503-6, 21503-8, 21503-10, 21504-6, 21504-8, 21504-10.     6. HLS Plate, Y-Shape; Article Numbers: 21513-3, 21513-5, 21514-3, 21514-5.     7. Locking Stabilization Screw; Article Numbers: 37151-5, 37151-8, 37151-9, 37151-10, 37151-12, 37151-13, 37151-15, 37151-16, 37151-18, 37151-24, 37251-8, 37251-9, 37251-11, 37251-12, 37251-13, 37251-14, 37251-16, 37251-20.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218338</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218338</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - I.T.S. Fibula Plate PROlock with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers.     1. Distal Tubular Plate; Article Numbers: 21602-3, 21602-4, 21602-5, 21602-6, 21602-7, 21602-8, 21603-3, 21603-4, 21603-5, 21603-6, 21603-7, 21603-8.     2. Fibula Plate 3.5mm; Article Numbers: 21225-4, 21225-6, 21225-8, 21225-10, 21225-12, 21226-4, 21226-6, 21226-8, 21226-10, 21226-12.     3. Universal Tubular Plate; Article Numbers: 21601-5, 21601-6, 21601-7, 21601-8, 21601-10, 21601-12, 21601-14, 21601-16.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218332</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218332</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - I.T.S. Pelvic Reconstruction System (PRS RX &amp; PRS Phoenix) - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: I.T.S. Pelvic Reconstruction System (PRS RX &amp; PRS Phoenix) with the below descriptions and corresponding article numbers.  1. Anterior Column Plate; Article Numbers: 21218-16, 21219-16.   2. Anterior Column Plate; Article Numbers: 21218-14, 21219-14.   3. Biplanar 2-Column Plate; Article Numbers: 21216-10, 21216-12, 21217-10, 21217-12.   4. Cancellous Screw; Article Numbers: 30591-36, 30591-70, 30591-75, 30591-80, 30591-85, 30591-90.  5. Cancellous Screw, Locking; Article Numbers: 37422-12-N, 37422-14-N, 37422-16-N, 37422-18-N, 37422-20-N, 37422-22-N, 37422-24-N, 37422-26-N, 37422-28-N, 37422-30-N, 37422-32-N, 37422-34-N, 37422-36-N, 37422-38-N, 37422-40-N, 37422-42-N, 37422-44-N, 37422-46-N, 37422-48-N, 37422-50-N, 37422-55-N, 37422-60-N, 37422-65-N, 37422-70-N, 37422-75-N, 37422-80-N, 37422-85-N, 37422-90-N, 37422-95-N, 37422-100-N, 37422-105-N, 37422-110-N, 37422-115-N, 37422-120-N, 37592-18, 37592-20, 37592-22, 37592-24, 37592-26, 37592-28, 37592-30, 37592-32, 37592-34, 37592-36, 37592-38, 37592-40, 37592-42, 37592-46, 37592-48, 37592-50, 37592-54, 37592-56, 37592-58, 37592-60, 37592-65, 37592-70, 37592-75, 37592-80, 37592-85, 37592-90.   6. Cannulated Screw, Cancellous; Article Numbers: 31851-60, 31851-65, 31851-70, 31851-75, 31851-80, 31851-85, 31851-90, 31851-95, 31851-100, 31851-105, 31851-110, 31851-115, 31851-120, 31851-125, 31851-130, 31851-135, 31851-140, 31851-145, 31851-150, 31851-155, 31851-160, 31851-165, 31851-170, 31851-175, 31851-180, 31851-185, 31851-190, 31851-195, 31851-200, 31854-60, 31854-65, 31854-70, 31854-75, 31854-80, 31854-85, 31854-90, 31854-95, 31854-100, 31854-105, 31854-110, 31854-115, 31854-120, 31854-125, 31854-130, 31854-135, 31854-140, 31854-145, 31854-150, 31854-155, 31854-160, 31854-165, 31854-170, 31854-175, 31854-180, 31854-185, 31854-190, 31854-195, 31854-200.   7. Cortical Screw; Article Numbers: 32351-10, 32351-12, 32351-14, 32351-16, 32351-18, 32351-20, 32351-22, 32351-24, 32351-26, 32351-28, 32351-30, 32351-32, 32351-34, 32351-36, 32351-38, 32351-40, 32351-42, 32351-44, 32351-46, 32351-48, 32351-50, 32351-55, 32351-60, 32351-65, 32351-70, 32351-75, 32351-80, 32351-85, 32352-16, 32352-18, 32352-20, 32352-22, 32352-24, 32352-26, 32352-28, 32352-30, 32352-32, 32352-34, 32352-36, 32352-38, 32352-40, 32352-42, 32352-44, 32352-46, 32352-48, 32352-50, 32352-55, 32352-60, 32352-65, 32352-70, 32352-75, 32352-80, 32352-85, 32352-90, 32352-95, 32352-100, 32352-105, 32352-110, 32352-115, 32352-120, 32455-18, 32455-20, 32455-22, 32455-24, 32455-26, 32455-28, 32455-30, 32455-32, 32455-34, 32455-36, 32455-38, 32455-40, 32455-42, 32455-44, 32455-46, 32455-48, 32455-50, 32455-52, 32455-54, 32455-56, 32455-58, 32455-60, 32455-65, 32455-70, 32455-75, 32455-80, 32455-85, 32455-90, 32475-32.   8. Cortical Screw, Locking; Article Numbers: 37455-18, 37455-20, 37455-22, 37455-24, 37455-26, 37455-28, 37455-30, 37455-32, 37455-34, 37455-36, 37455-38, 37455-40, 37455-42, 37455-44, 37455-46, 37455-48, 37455-50, 37455-52, 37455-54, 37455-56, 37455-60, 37455-65, 37455-70, 37455-75, 37455-80, 37455-85, 37455-90.   9. Curved Plate; Article Numbers: 211911-4, 211911-5, 211911-6, 211911-7, 211911-8, 211911-10, 211911-12, 211911-14, 211911-16, 211911-20.   10. Posterior Column Plate, Left; Article Numbers: 212121-6.   11. Posterior Column Plate, Right; Article Numbers: 212131-6.   12. Posterior Wall Plate, Extended, Left; Article Numbers: 212101-SM.   13. Posterior Wall Plate, Extended, Left; Article Numbers: 212101-LA.   14. Posterior Wall Plate, Extended, Right; Article Numbers: 212111-LA, 212111-SM.   15. Posterior Wall Plate, Left; Article Numbers: 212141-7, 212141-8.   16. Posterior Wall Plate, Right; Article Numbers: 212151-7, 212151-8.   17. PRS Plate; Article Numbers: 21194-6, 21194-7, 21194-8, 21195-10, 21195-12, 21195-7.   18. Quadrilateral Buttress Plate; Article Numbers: 21208-13, 21209-13.   19. Quadrilateral Buttress Plate; Article Numbers: 21208-11, 21209-11.   20. Rim Plate, Left; Article]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218339</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218339</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Pelvic Reconstruction System (PRS) - Class 2 Recall]]></title>
				<description><![CDATA[Pelvic Reconstruction System (PRS) with the below descriptions and corresponding article numbers.     1. Fixation Screw; Article Number: 70312.     2. Spike short; Article Number: 70314.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218331</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218331</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - I.T.S. DUL (Distal Ulna Locking) System, UOL (Ulna Osteotomy Locking) System - Class 2 Recall]]></title>
				<description><![CDATA[I.T.S. DUL (Distal Ulna Locking) System and UOL (Ulna Osteotomy Locking) System with the below descriptions and corresponding article numbers.  1. I.T.S. DUL (Distal Ulna Locking) System, Distal Ulna Plate; Article Numbers: 21232-3, 21232-4, 21232-6, 21233-3, 21233-4, 21233-6, 21234-4, 21235-4.   2. I.T.S. UOL (Ulna Osteotomy Locking) System, Ulna Osteotomy Plate; Article Numbers: 21231-6.   3. UOL (Ulna Osteotomy Locking) System, Cancellous Screw, Locking; Article Numbers: 37302-18, 37302-20.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218335</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218335</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - HCS  Headless Compression Screw System - Class 2 Recall]]></title>
				<description><![CDATA[HCS - Headless Compression Screw System, Headless Compression Screw, Cannulated; Article Numbers: 31207-10, 31207-12, 31207-14, 31207-16, 31207-18, 31207-20, 31207-24, 31207-26, 31207-28, 31207-30, 31257-12, 31257-14, 31257-16, 31257-18, 31257-20, 31257-22, 31257-24, 31257-28, 31257-30, 31307-18, 31307-32, 31307-34, 31307-36, 31307-38, 31358-30, 31437-30, 31437-38, 31437-40, 31437-50, 31757-100, 31757-120, 31757-45, 31757-80, 31757-85, 31757-90.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218337</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218337</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Humeral Head Plate with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Humeral Head Plate with Angular Stability, with the following description: Proximal Humeral Plate. Article Numbers: 211341-10, 211341-4, 211341-7, 21134-4, 21134-5, 21135-4, 21136-4, 21136-5, 21136-7, 21137-4, 21137-7, 21138-4, 21139-4.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218325</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218325</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - I.T.S. LRS (Locking Reconstruction System) DFL (Distal Femur Locking), I.T.S. LRS (Locking Reconstruction Sys - Class 2 Recall]]></title>
				<description><![CDATA[I.T.S. LRS (Locking Reconstruction System) with the below descriptions and corresponding article numbers.     1. DFL (Distal Femur Locking) Distal Femur Plate; Article Numbers: 21301-5, 21301-7, 21301-9, 21301-13, 21302-5, 21302-7, 21302-9, 21302-13.     2. PTL (Proximal Lateral Tibia Locking) Proximal Lateral Tibia Plate; Article Numbers: 21321-7, 21321-12, 21322-7, 21322-12.     3.PTL (Proximal Lateral Tibia Locking) Proximal Medial Tibia Plate; Article Numbers: 21325-4, 21325-7.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218334</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218334</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - I.T.S. Straight Plate with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[I.T.S. Straight Plate with Angular Stability with the below descriptions and corresponding article numbers.     1. Forearm Plate, Curved; Article Numbers: 21604-6, 21604-9.     2. Forearm Plate, Straight; Article Numbers: 21605-11, 21605-6, 21605-9.    3. Straight Compression Plate; Article Numbers: 21105-6, 21105-8.    4. Straight Plate, 1.5mm; Article Numbers: 21104-4, 21104-5, 21104-6, 21104-7, 21104-8, 21104-9.    5. Straight Plate, 2.0mm; Article Numbers: 21101-5, 21101-6, 21101-7, 21101-8, 21101-9, 21101-11, 21101-13.    6. Straight Plate, 3.5mm; Article Number: 21102-6.     7. Straight Plate, 4.5mm; Article Numbers: 21103-8, 21103-11, 21103-10, 21103-11, 21103-12, 21103-13, 21103-8, 21103-9.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218329</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218329</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Olecranonplate with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[Olecranonplate with Angular Stability with the below descriptions and corresponding article numbers.    1. Olecranon Hook Plate; Article Numbers: 21112-7, 21114-5, 21113-9.    2. Olecranon Plate; Article Numbers: 21111-6, 21111-8, 21111-12.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218328</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218328</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Volar Radius Plate with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[Volar Radius Plate with Angular Stability with the following description: Radius Plate PROlock II. Article Numbers: 21031-3, 21031-5, 21032-11, 21032-3, 21032-5, 21033-3, 21033-5, 21034-3, 21034-5, 21035-3, 21036-3.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218323</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218323</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Claviculaplate with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[Claviculaplate with Angular Stability, with the below descriptions and associated article numbers.     1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10.     2. Clavicle Plate; Article Numbers: 21121-6, 21121-8.     3. Clavicle Plate, 3.5mm; Article Numbers: 21122-10, 21122-6, 21122-8.     4. Clavicle Plate, Lateral; Article Numbers: 21123-4, 21124-4, 21127-6, 21128-6.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218324</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218324</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Distal Humeral Plates with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers.     1. Cortical Screw, Locking; Article Numbers: 37351-10-N, 37351-12-N, 37351-14-N, 37351-16-N, 37351-18-N, 37351-20-N, 37351-22-N, 37351-24-N, 37351-26-N, 37351-28-N, 37351-30-N, 37351-32-N, 37351-34-N, 37351-36-N, 37351-38-N, 37351-40-N, 37351-42-N, 37351-44-N, 37351-46-N, 37351-48-N, 37351-50-N, 37351-55-N, 37351-60-N, 37351-65-N, 37351-70-N, 37351-75-N, 37351-80-N, 37351-85-N.     2. Humeral Plate, Distal; Article Numbers: 21241-5, 21241-7, 21242-7, 21243-10, 21244-9.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218333</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218333</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - FLS  Foot Locking Plates System, HOL  Hallux Osteotomy Locking Plate - Class 2 Recall]]></title>
				<description><![CDATA[FLS - Foot Locking Plates System and HOL - Hallux Osteotomy Locking Plate with the below descriptions and corresponding article numbers.     1. FLS - Foot Locking Plates System, Cancellous Stabilization Screw; Article Numbers: 37303-10, 37303-12, 37303-14, 37303-16, 37303-18, 37303-20, 37303-22, 37303-24, 37303-26, 37303-28, 37303-30.     2. FLS - Foot Locking Plates System, Cortical Screw; Article Numbers: 32271-10, 32271-12, 32271-14, 32271-16, 32271-18, 32271-20, 32271-22, 32271-24, 32271-26, 32271-28, 32271-32, 32271-34.     3. FLS - Foot Locking Plates System, Cortical Stabilization Screw; Article Numbers: 37304-10, 37304-12, 37304-14, 37304-16, 37304-18, 37304-20, 37304-22, 37304-24.     4. FLS - Foot Locking Plates System, FLS Plate, Curved; Article Numbers: 21413-6.     5. FLS - Foot Locking Plates System, FLS Plate, H-Shape; Article Numbers: 21431-ME.     6. FLS - Foot Locking Plates System, FLS Plate, L-Shape; Article Numbers: 21482, 21483.     7. FLS - Foot Locking Plates System, FLS Plate, Straight; Article Numbers: 21421-5.     8. FLS - Foot Locking Plates System, Stabilization Screw; Article Numbers: 37241-10, 37241-12, 37241-14, 37241-16, 37241-18, 37241-20, 37241-22, 37241-24, 37241-26, 37241-28, 37241-30.     9. HOL - Hallux Osteotomy Locking Plate, Hallux Osteotomy Plate; Article Numbers: 21015-08, 21015-09.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218336</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218336</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - Pilonplate with Angular Stability - Class 2 Recall]]></title>
				<description><![CDATA[Pilonplate with Angular Stability, with the below descriptions and corresponding article numbers.     1. Anterolateral Tibia Plate; Article Numbers: 21311-11, 21311-15, 21311-7, 21312-11, 21312-15, 21312-7.     2. Pilon Plate 4mm; Article Numbers: 21094-10, 21094-4, 21094-6, 21094-8.    3. Pilon Plate, Small; Article Numbers: 21093-4, 21093-6.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218327</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218327</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - FR.O.H. Calcaneus Repair System - Class 2 Recall]]></title>
				<description><![CDATA[FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218326</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218326</guid>
			</item>
	
	
			<item>
				<title><![CDATA[I.T.S. GmbH - I.T.S. Screw System - Class 2 Recall]]></title>
				<description><![CDATA[I.T.S. Screw System with the below descriptions and corresponding article numbers.     1. Cancellous Screw, Cannulated; Article Numbers: 31404-16, 31404-18, 31404-20, 31404-22, 31404-24, 31404-26, 31404-28, 31404-30, 31404-32, 31404-34, 31404-36, 31404-38, 31404-40, 31404-42, 31404-44, 31404-46, 31404-48, 31404-50, 31404-55, 31404-60, 31404-65, 31404-70, 31404-75, 31404-80, 31457-30, 31457-36, 31457-40, 31457-46, 31457-50, 31457-55, 31457-60, 31652-100, 31652-105, 31652-110, 31652-115, 31652-120, 31652-25, 31652-30, 31652-35, 31652-40, 31652-45, 31652-55, 31652-60, 31652-65, 31652-70, 31652-75, 31652-80, 31652-85, 31652-90, 31652-95, 31731-100, 31731-105, 31731-110, 31731-115, 31731-120, 31731-50, 31731-60, 31731-65, 31731-70, 31731-75, 31731-80, 31731-85, 31731-90, 31731-95, 31732-60, 31734-100, 31734-105, 31734-110, 31734-115, 31734-120, 31734-45, 31734-50, 31734-60, 31734-65, 31734-70, 31734-75, 31734-80, 31734-85, 31734-90, 31734-95.    2. Cortical Screw, Cannulated; Article Numbers: 31357-44, 31357-22, 31357-48, 31277-18, 31357-20, 31357-22, 31357-24, 31357-26, 31357-28, 31357-30, 31357-32, 31357-34, 31357-36, 31357-38, 31357-40, 31357-42, 31357-44, 31357-46, 31357-48, 31357-60, 31357-65, 31357-70.     3. Washer; Article Number: 36851.    4. Washer, Concave; Article Numbers: 36432, 36653, 36732.     5. Washer, Flat; Article Numbers: 36431, 36651, 36653, 36731.]]></description>
				<pubDate>Sat, 21 Mar 2026 01:06:58 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218330</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218330</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Diagnostica Stago, Inc. - STA Liatest DDi - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: STA Liatest D-Di  Product Name: STA Liatest D-Di  Model/Catalog Number: REF 00515  Product Description: The STA&#xbf; - Liatest &#xbf; D-Di kit is an immuno-turbidimetric assay for the quantitative determination of D-dimer in venous plasma (in 3.2 % sodium citrate) for use on STA-R&#xbf;, STA Compact&#xbf; and STA Satellite&#xbf; analyzers by   professional laboratory personnel. The STA&#xbf; - Liatest&#xbf; D-Di is intended for use in conjunction with a clinical pretest probability (PTP) assessment model to exclude pulmonary embolism (PE) and deep venous thrombosis (DVT) in outpatients suspected of PE or DVT.  Component: No]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:55 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218462</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218462</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConvaTec, Inc - Convatec, EsteemBody Drainable Pouch - Class 2 Recall]]></title>
				<description><![CDATA[Convatec, EsteemBody Drainable Pouch  REF:423643,   10-45mm]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218805</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218805</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConvaTec, Inc - Convatec, EsteemBody Drainable Pouch - Class 2 Recall]]></title>
				<description><![CDATA[Convatec, EsteemBody Drainable Pouch  REF:423653  10-35mm]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218808</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218808</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConvaTec, Inc - Convatec, EsteemBody Drainable Pouch - Class 2 Recall]]></title>
				<description><![CDATA[Convatec, EsteemBody Drainable Pouch  REF:423657  10-35mm]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:53 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218809</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218809</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hologic, Inc. - Aptima HPV Assay - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Aptima HPV Assay  Product Name: Aptima HPV Assay  Model/Catalog Number: 303585  Product Description: Aptima HPV assay  Component: No]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:29 GMT</pubDate>
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				<title><![CDATA[Elekta, Inc. - Leksell Gamma Knife - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Leksell Gamma Knife  Product Description: Leksell Gamma Knife&#xbf; Perfexion  Leksell Gamma Knife&#xbf; Icon&quot;  Leksell Gamma Knife&#xbf;   Elekta Esprit      Leksell Gamma Knife&#xbf; (available models Elekta Esprit, Icon&quot;, and Perfexion&quot;) is a radiosurgery system for use in the stereotactic irradiation of head structures. Surgery is achieved by delivering a prescribed dose as one or more shots of ionizing radiation to the exact site of the target.]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:27 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218768</link>
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			<item>
				<title><![CDATA[Stryker Medical Division of Stryker Corporation - Cub Pediatric Crib - Class 2 Recall]]></title>
				<description><![CDATA[Cub Pediatric Crib, Model FL19H]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218684</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218684</guid>
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			<item>
				<title><![CDATA[LeMaitre Vascular, Inc. - Artegraft Vascular Graft - Class 2 Recall]]></title>
				<description><![CDATA[Artegraft Vascular Graft;  REF#: AG740;]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:23 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218639</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218639</guid>
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			<item>
				<title><![CDATA[Howmedica Osteonics Corp. - MICS3 - Class 2 Recall]]></title>
				<description><![CDATA[MICS3 Angled Sagittal Saw Attachment;  Part Number: 210490]]></description>
				<pubDate>Thu, 19 Mar 2026 01:06:35 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218642</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218642</guid>
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			<item>
				<title><![CDATA[Baxter Healthcare Corporation - Welch Allyn, Inc. - Class 2 Recall]]></title>
				<description><![CDATA[Brand Name: Welch Allyn, Inc.  Product Name: Welch Allyn Spot Vision Screener VS100  Model/Catalog Number: VS100  Software Version: Software version 3.2.0.1  Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic  One unit per package]]></description>
				<pubDate>Thu, 19 Mar 2026 01:06:33 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218746</link>
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			<item>
				<title><![CDATA[Philips Ultrasound, Inc - Philips L125 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips L12-5 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218875</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips S41 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips S4-1 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218880</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips Mini Multi TEE Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips Mini Multi TEE Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218877</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips X31 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips X3-1 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218882</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218882</guid>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips OMNI III TEE Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips OMNI III TEE Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218879</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips 3D62 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips 3D6-2 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218873</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips C94 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips C9-4 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218874</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips S52 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips S5-2 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218881</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips X72 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips X7-2 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218883</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips L175 Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips L17-5 Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218876</link>
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				<title><![CDATA[Philips Ultrasound, Inc - Philips OMNI II TEE Ultrasound Transducer - Class 3 Recall]]></title>
				<description><![CDATA[Philips OMNI II TEE Ultrasound Transducer]]></description>
				<pubDate>Wed, 25 Mar 2026 01:07:25 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218878</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218878</guid>
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				<title><![CDATA[Datascope Corp. - Battery Charging Station - Class 3 Recall]]></title>
				<description><![CDATA[Battery Charging Station;  Model: 0998-00-0802;]]></description>
				<pubDate>Fri, 20 Mar 2026 01:06:31 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=218716</link>
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