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			<title>Medical Device Recalls since May 13, 2013</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>Mon, 20 May  2013 04:34:02 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[Cook, Inc. - Zilver PTX DrugEluting Peripheral Stent - Class 1 Recall]]></title>
				<description><![CDATA[Zilver&#xbf; PTX&#xbf; Drug-Eluting Peripheral Stent - 6 mm X 80mm; 125 cm, Rx, Sterile    Product Usage:  The Zilver PTX Drug -Eluting Peripheral Stent is a self expanding, small metal, mesh tube (stent) with the outer surface coated with the drug Paclitaxel that can be Implanted in an artery in the thigh (femoropopliteal artery). The Paclitaxel coating helps Preven the artery from narrowing again (restenosis). The Zilver; PTX stent acts as a scaffold to:   Hold open a narrowed artery in the thigh (femoropopliteal artery) caused by PAD .   improve blood flow to the extremity.]]></description>
				<pubDate>Thu, 16 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117571</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117571</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cook, Inc. - Zilver PTX DrugEluting Peripheral Stent - Class 1 Recall]]></title>
				<description><![CDATA[Zilver PTX Drug-Eluting Peripheral Stent, - 7 mm X 80mm; 125 cm, Rx, Sterile    Product Usage:  The Zilver PTX Drug -Eluting Peripheral Stent is a self expanding, small metal, mesh tube (stent) with the outer surface coated with the drug Paclitaxel that can be Implanted in an artery in the thigh (femoropopliteal artery). The Paclitaxel coating helps prevent the artery from narrowing again (restenosis). The Zilver; PTX stent acts as a scaffold to: Hold open a narrowed artery in the thigh (femoropopliteal artery) caused by PAD. Improve blood flow to the extremity.]]></description>
				<pubDate>Thu, 16 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117653</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117653</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Abbott Diabetes Care, Inc. - FreeStyle InsuLinx Blood Glucose Monitoring System - Class 1 Recall]]></title>
				<description><![CDATA[FreeStyle InsuLinx Blood Glucose Monitoring System:  For In Vitro Diagnostic Use only. Use only with FreeStyle InsuLinx test strips.    Abbott Diabetes Care, Inc.  1360 South Loop Road  Alameda, CA 94502 USA    The FreeStyle InsuLinx Blood Glucose Test Strips are for use with the FreeStyle InsuLinx Blood Glucose Meter to quantitatively measure glucose in capillary whole blood samples drawn from the fingertip.]]></description>
				<pubDate>Fri, 10 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117228</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117228</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Total Hip, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Total Hip, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116920</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116920</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Knee Arthroscopy, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Knee Arthroscopy, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116915</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116915</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Extremity, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Extremity, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116916</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116916</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Hand, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Hand, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116917</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116917</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS - Class 1 Recall]]></title>
				<description><![CDATA[A) Presource PBDS, Lap Chole, Kit, Clean Up;   B) Presource PBDS, Greenwood LeFlore Hosp, Lap Chole, Kit]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116912</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116912</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Gyn Laparoscopy Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Gyn Laparoscopy Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116902</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116902</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Knee Arthroscopy, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Knee Arthroscopy, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117005</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117005</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Total Knee, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Total Knee, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116922</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116922</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Major Abdominal, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Major Abdominal, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116914</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116914</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Shoulder Arthroscopy, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Shoulder Arthroscopy, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116918</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116918</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Total Joint, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Total Joint, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116921</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116921</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Beaufort Memorial Hospital, Anesthesia Circuit, Kit - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Beaufort Memorial Hospital, Anesthesia Circuit, Kit]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116923</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116923</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, General Laparoscopy, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, General Laparoscopy, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116913</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116913</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cardinal Health, Medical Products &amp; Services - Presource PBDS, Shoulder Procedure, Kit, Circulator - Class 1 Recall]]></title>
				<description><![CDATA[Presource PBDS, Shoulder Procedure, Kit, Circulator]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116919</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116919</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Neuromodulation - Activa Dystonia Therapy Kit - Class 1 Recall]]></title>
				<description><![CDATA[Medtronic DBS Therapy for Dystonia Kit,  models 3317, 3319, 3337 and 3339.  Sterile and Non-Pyrogenic.       Product Usage:  Dystonia Therapy Kit is indicated for unilateral or bilateral stimulation of the internal globus pallidus (GPi) or the subthalamic nucleus (STN) to aid in the management of chronic, intractable (drug refractory) primary dystonia, including generalized and/or segmental dystonia, hemidystonia, and cervical dystonia (torticollis).]]></description>
				<pubDate>Thu, 02 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117824</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117824</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtronic Neuromodulation - Deep Brain Stimulation Lead Kit - Class 1 Recall]]></title>
				<description><![CDATA[Medtronic DBS Lead Kit for Deep Brain Stimulation, models 3387, 3387S, 3389, 3389S, 3391, 3391S.  Sterile and Non-Pyrogenic.    Product Usage:    The deep brain stimulation system delivers electrical stimulation to selected targets in the brain. DBS Leads are indicated for Dystonia, Essential Tremor (ET), Obsessive-Compulsive Disorder (OCD), Parkinson s Disease (PD), and epilepsy.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116147</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116147</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hospira Inc. - GemStar Infusion System - Class 1 Recall]]></title>
				<description><![CDATA[The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two disposable AA alkaline batteries. When powered by batteries, The GemStar Pump is ideal for ambulatory patients.    The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required.]]></description>
				<pubDate>Wed, 01 May 2013 01:00:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117159</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117159</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hospira Inc. - GemStar Infusion System - Class 1 Recall]]></title>
				<description><![CDATA[The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two disposable AA alkaline batteries. When powered by batteries, The GemStar Pump is ideal for ambulatory patients.    The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required.]]></description>
				<pubDate>Wed, 01 May 2013 01:00:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117216</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117216</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Newport Medical Instruments Inc - Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries - Class 1 Recall]]></title>
				<description><![CDATA[Newport Medical Instruments HT70  and HT70 Plus ventilator Power Pac batteries  Model number: HT70 and HT70 Plus.     The HT70 and HT70 Plus ventilator systems are intended to provide continuous or intermittent positive pressure mechanical ventilatory support for the care of individuals who require mechanical ventilation through invasive or non-invasive interfaces.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117179</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117179</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Maquet Cardiovascular Us Sales, Llc - SERVOi ventilator system - Class 1 Recall]]></title>
				<description><![CDATA[Maquet Getinge Group battery modules for use with Maquet SERVO-i ventilator systems (Part #6487180).    Battery for use with the SERVO-i Ventilator System. The SERVO-i Ventilator System is intended for treating and monitoring patients ranging from neonates to adults with respiratory failure or insufficiency. The ventilator is equipped with at least 2, NiMH battery modules (Part No. 6487180) which automatically supply 12V DC Power in case of an AC power failure, ensuring that ventilator settings and stored data remain intact in the event of an AC power failure. The battery modules give the user a possibility to use the SERVO-i during intra-hospital transportation.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116703</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116703</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hospira Inc. - GemStar Infusion System - Class 1 Recall]]></title>
				<description><![CDATA[GemStar Pump  - Battery      Product Usage:  The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two disposable AA alkaline batteries. When powered by batteries, The GemStar Pump is ideal for ambulatory patients.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117160</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117160</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hospira Inc. - GemStar Infusion System - Class 1 Recall]]></title>
				<description><![CDATA[GemStar Pump  - Battery    Product Usage:  The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the home, in the hospital, or anywhere electronic infusion is required. The GemStar Pump can be powered by AC mains adaptor, rechargeable battery pack, docking station, or two disposable AA alkaline batteries. When powered by batteries, The GemStar Pump is ideal for ambulatory patients.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117195</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117195</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Johnson &amp; Johnson Vision Care, Inc. - 1DAy ACUVUE MOIST contact lens - Class 2 Recall]]></title>
				<description><![CDATA[1-DAY ACUVUE MOIST Brand Contact Lenses, soft disposable contact lenses.    The Vistakon (etafilcon A) Soft (hydrophilic) Contact Lens, Clear and Tinted (Visibility and/or Cosmetically), with UV Blocker for Daily Disposable Wear (spherical) is indicated for daily wear to enhance or alter the apparent color of the eye and/or for the correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with not diseased eyes who may have 1.00D or less of astigmatism.]]></description>
				<pubDate>Sat, 18 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116214</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116214</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Johnson &amp; Johnson Vision Care, Inc. - ACUVUE ADVANCE Brand Contact Lens - Class 2 Recall]]></title>
				<description><![CDATA[ACUVUE ADVANCE Brand Contact Lenses with HYDRACLEAR, Soft, disposable contact lenses.    The Vistakon (galyfilcon A) Contact Lens is indicated for daily wear for the correction of refractive ametropia (myopia and hyperopia) in aphakic or non-aphakic persons with non-diseased eyes who may have 1.00D of astigmatism or less.]]></description>
				<pubDate>Sat, 18 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116215</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116215</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hologic, Inc. - Fluoroscan Mini Carm InSight, software versions 1.x, 2.x, 3.x - Class 2 Recall]]></title>
				<description><![CDATA[Fluoroscan Mini C-arm InSight, software versions 1.x, 2.x, 3.x    The device is a Mini C-arm Fluroscopic Imaging System designed to provide physicians with general fluoroscopic visualization of a patient, including but no limited to surgical orthopedic and podiatry use, critical and emergency procedures, and light anatomy imaging situation.]]></description>
				<pubDate>Sat, 18 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117689</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117689</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Hologic, Inc. - Fluoroscan Mini Carm InSight2, software versions 3.x, 4.0, 4.0.1, 4.0.2 - Class 2 Recall]]></title>
				<description><![CDATA[Fluoroscan Mini C-arm InSight2, software versions 3.x, 4.0, 4.0.1, 4.0.2    The device is a Mini C-arm Fluroscopic Imaging System designed to provide physicians with general fluoroscopic visualization of a patient, including but no limited to surgical orthopedic and podiatry use, critical and emergency procedures, and light anatomy imaging situation.]]></description>
				<pubDate>Sat, 18 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117690</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117690</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Co. - BBL Trypticase Soy Agar with 5 Sheep Blood and MacConkey III Plate - Class 2 Recall]]></title>
				<description><![CDATA[BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood and MacConkey II-I Plate.    Used for culturing microorganisms.]]></description>
				<pubDate>Fri, 17 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117273</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117273</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Co. - BBL CDC Anaerobe 5 Sheep Blood Agar. - Class 2 Recall]]></title>
				<description><![CDATA[BBL(tm) CDC Anaerobe 5% Sheep Blood Agar.    Used for culturing microorganisms.]]></description>
				<pubDate>Fri, 17 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117274</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117274</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Co. - BBL Trypticase Soy Agar with 5 Sheep Blood - Class 2 Recall]]></title>
				<description><![CDATA[BBL(tm) Trypticase (tm) Soy Agar with 5% Sheep Blood.    Used for culturing microorganisms.]]></description>
				<pubDate>Fri, 17 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117272</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117272</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medtox Diagnostics Inc - PROFILEV MEDTOXScan Drugs of Abuse Test System - Class 2 Recall]]></title>
				<description><![CDATA[PROFILE-V MEDTOXScan Drugs of Abuse Test System.    For the rapid, qualitative detection of drugs of abuse in human urine,]]></description>
				<pubDate>Fri, 17 May 2013 01:00:13 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117098</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117098</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Varian Medical Systems, Inc. Oncology Systems - Varian High Energy Clinacs - Class 2 Recall]]></title>
				<description><![CDATA[Varian High Energy Clinacs, High Energy Accelerator, Radiation Treatment System, Model Numbers: H14, H27,H29, HCX,     Product Usage:  The Varian High Energy Accelerator is intended to provide stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.]]></description>
				<pubDate>Thu, 16 May 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117604</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117604</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Iris Diagnostics - Iris Diagnostics Division iQ Control/Focus Set - Class 2 Recall]]></title>
				<description><![CDATA[Iris Diagnostics Division iQ Control/Focus Set, Part Number 800-3104, Lot Number 153-12.    Product Usage:  For in vitro diagnostic use with the iQ200 series.]]></description>
				<pubDate>Thu, 16 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117370</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117370</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Varian Medical Systems, Inc. - Segmented Cylinder Applicator Set - Class 2 Recall]]></title>
				<description><![CDATA[Segmented Cylinder Applicator Set, Model # GM11004150, when used for Pulsed Dose Rate (PDR)    Product Usage:  Usage:  Used during pulsed dose rate brachytherapy to treat vaginal and rectal cancer.]]></description>
				<pubDate>Thu, 16 May 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117584</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117584</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Heartware Inc - HVAD Pump Implant Kit - Class 2 Recall]]></title>
				<description><![CDATA[REF 1103***HVAD Pump Implant Kit.    Used as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure.]]></description>
				<pubDate>Wed, 15 May 2013 01:00:18 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=115985</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=115985</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innov - Class 2 Recall]]></title>
				<description><![CDATA[GE Healthcare Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ, Innova 2121 IQ, Innova 3131 IQ , Innova 3100, Innova 4100.    For use in generating fluoroscopic images of human anatomy for diagnostic and interventional procedures.]]></description>
				<pubDate>Wed, 15 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117691</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117691</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Edwards Lifesciences, LLC - Proplege Coronary Sinus Catheter - Class 2 Recall]]></title>
				<description><![CDATA[Proplege Coronary Sinus Catheter model PR9, 11 French Introducer, kitted with PR9.    Product Usage:  The catheter introducer sheath kit provides access to the central venous circulation to facilitate catheter and guidewire insertion. The Proplege coronary sinus catheter provides retrograde cardioplegia during cardiopulmonary by-pass surgery.]]></description>
				<pubDate>Wed, 15 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=115620</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=115620</guid>
			</item>
	
	
			<item>
				<title><![CDATA[QIAGEN Gaithersburg, Inc. - Qiagen artus CMV RG PCR ASR (Analyte Specific Reagent) - Class 2 Recall]]></title>
				<description><![CDATA[QIAGEN artus CMV RG PCR ASR (24) (Catalog number 4503223)     Product Usage:  The artus CMV RG PCR ASR  is designed to detect and to quantify nucleic acid specific to human cytomegalovirus (CMV) using real-time  PCR technology (PCR) in the Rotor-Gene 2000/3000 (RG).]]></description>
				<pubDate>Wed, 15 May 2013 01:00:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116823</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116823</guid>
			</item>
	
	
			<item>
				<title><![CDATA[QIAGEN Gaithersburg, Inc. - Qiagen artus CMV RG PCR ASR - Class 2 Recall]]></title>
				<description><![CDATA[QIAGEN artus CMV RG PCR ASR (96) (Catalog number 4503225)     Product Usage:  Test is intended for use in the detection and quantitation of human cytomegalovirus (CMV) specific DNA, as part of an in house validated real-time PCR assay.  One service package containing the handbook.]]></description>
				<pubDate>Wed, 15 May 2013 01:00:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116716</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116716</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Summit Medical, Inc. - Summit Medical, BL2006, Myringotomy Lance (Juvenile) Blade - Class 2 Recall]]></title>
				<description><![CDATA[Summit Medical, BL-2006, Myringotomy Lance (Juvenile) Blade, Sterile P, Summit Medical, Inc., 815 Northwest Parkway, Suite 100, St. Paul, MN 55121    Use to make an incision in the tympanic membrane.]]></description>
				<pubDate>Wed, 15 May 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117723</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117723</guid>
			</item>
	
	
			<item>
				<title><![CDATA[ConMed Corporation - PadPro(R) Adult Radiotransparent Multifunction Electrodes - Class 2 Recall]]></title>
				<description><![CDATA[PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C.     The PadPro(R) Adult Radiotransparent Multifunction Electrodes with Carbon Leadwires and Medtronic(R) Connector are intended to be used in external pacing, defibrillation and monitoring applications]]></description>
				<pubDate>Tue, 14 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117902</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117902</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Loop, Cutting - Class 2 Recall]]></title>
				<description><![CDATA[Loop, Cutting, Angled 22FR (26055G/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90682</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90682</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, Cutting - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, Cutting, 24FR, 0.30MM (27040G-.30/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90681</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90681</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, VaporCut - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, VaporCut, 24FR (27050SG/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90677</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90677</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Knife, Cold, Straight - Class 2 Recall]]></title>
				<description><![CDATA[Knife, Cold, Straight (27068K/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90680</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90680</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz  Electrode, cutting - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, cutting, 24FR (27050G/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90660</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90660</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, Roller Ball - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, Roller Ball, 24FR (27050NK/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90664</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90664</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, cutting - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, cutting, 24FR (27050G-.30/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90661</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90661</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, Roller, Vaporization - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, Roller, Vaporization, 24FR (27050RK/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90676</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90676</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, Barrel Bar - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, Barrel Bar, 24FR (27050NX/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90665</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90665</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, Coag, Pointed - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, Coag, Pointed, 24FR (27050L/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90662</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90662</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Loop, Cutting - Class 2 Recall]]></title>
				<description><![CDATA[Loop, Cutting, 24FR (26050G/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90678</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90678</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Electrode, Coag, Ball End - Class 2 Recall]]></title>
				<description><![CDATA[Electrode, Coag, Ball End, 24FR (27050N/6).    Resectoscope accessories (ie. electrode, cutting loops and cold knives).]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90663</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=90663</guid>
			</item>
	
	
			<item>
				<title><![CDATA[American Medical Systems, Inc. - AMS 800 Urinary Control System. - Class 2 Recall]]></title>
				<description><![CDATA[AMS 800&#xbf; Urinary Control System.      The AMS 800&#xbf; Urinary Control System is used to treat urinary incontinence due to reduced outlet resistance (intrinsic sphincter deficiency) following prostate surgery. The AMS 800&#xbf; Urinary Control System is an implantable, fluid filled, solid silicone elastomer device used to treat stress urinary incontinence. It is designed to restore the natural process of urinary control. The device simulates normal sphincter function by opening and closing the urethra at the control of the patient. The AMS 800 system consists of three inter connected components: a cuff, a pump, and a pressure-regulating balloon. The three components are connected with kink-resistant tubing. The AMS 800 can be implanted at either the bulbous urethra or the bladder neck.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117226</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117226</guid>
			</item>
	
	
			<item>
				<title><![CDATA[American Medical Systems, Inc. - AMS 800 Urinary Control System - Class 2 Recall]]></title>
				<description><![CDATA[AMS 800&#xbf; Urinary Control System.     The AMS 800&#xbf; Urinary Control System is used to treat urinary incontinence due to reduced outlet resistance (intrinsic sphincter deficiency) following prostate surgery. The AMS 800&#xbf; Urinary Control System is an implantable, fluid filled, solid silicone elastomer device used to treat stress urinary incontinence. It is designed to restore the natural process of urinary control. The device simulates normal sphincter function by opening and closing the urethra at the control of the patient. The AMS 800 system consists of three inter connected components: a cuff, a pump, and a pressure-regulating balloon. The three components are connected with kink-resistant tubing. The AMS 800 can be implanted at either the bulbous urethra or the bladder neck.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117227</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117227</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - BioMend Extend Absorbable Collagen Membrane - Class 2 Recall]]></title>
				<description><![CDATA[BioMend&#xbf; Extend&quot; Absorbable Collagen Membrane    BioMend&#xbf; Extend&quot; Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117061</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117061</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - Absorbable Collagen Sponge - Class 2 Recall]]></title>
				<description><![CDATA[Absorbable Collagen Sponge    Provided As Intermediate to Another Company]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117656</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117656</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - DuraGen XS Dural Regeneration Matrix - Class 2 Recall]]></title>
				<description><![CDATA[DuraGen XS Dural Regeneration Matrix    DuraGen XS Dural Regenerative Matrix is an absorbable implant for repair of dural defects. DuraGen XS is an easy to handle, soft, white, pliable, non-friable, porous collagen matrix. DuraGen XS is supplied sterile, non-pyrogenic, for single use in double peel packages in a variety of sizes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117041</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117041</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - DuraGen Suturable DuraGen Dural Regenerative Matrix - Class 2 Recall]]></title>
				<description><![CDATA[Suturable DuraGen Dural Regenerative Matrix    Suturable DuraGen Dural Regenerative Matrix is an absorbable implant for repair of dural defects. Suturable DuraGen is an easy to handle, soft, white, pliable, nonfriable, porous collagen matrix with a mechanically strengthened collagen component. Suturable DuraGen is supplied sterile, non-pyrogenic, for single use in double peel packages in a variety of sizes. Suturable DuraGen may be applied using either on-lay or suturing techniques depending on clinical need and surgeon preference.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117039</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117039</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - Helitene Absorbable Collagen Hemostatic Sponge - Class 2 Recall]]></title>
				<description><![CDATA[Helitene Absorbable Collagen Hemostatic Sponge    Helitene is indicated in surgical procedures (other than ophthalmological and urological surgery) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117047</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117047</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - CollaPlug Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[CollaPlug Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117050</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117050</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - CollaTape Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117048</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117048</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - NeuraGen Nerve Guide - Class 2 Recall]]></title>
				<description><![CDATA[NeuraGen Nerve Guide    NeuraGen Nerve Guide is indicated for repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117043</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117043</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - Helistat Absorbable Hemostatic,Collagen Based - Class 2 Recall]]></title>
				<description><![CDATA[Helistat Absorbable Hemostatic,Collagen Based    Helistat is indicated in surgical procedures (other than ophthalmological and urological surgery) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117046</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117046</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Insight Instruments, Inc. - Insight Instruments MIS ( MultiPort Illumination System) - Class 2 Recall]]></title>
				<description><![CDATA[Insight Instruments MIS ( Multi-Port Illumination System)      Illuminated pilot tubes work like a ceiling light while simultaneously protecting the entry sites. Illumination automatically follows the movement of the two surgical instruments inserted into the M.I.S. cannulas. The large distance of more than 16mm between cannula ends and posterior pole guarantees sufficient light in the working area and a large observation field especially when used in conjunction with modern wide field panoramic observation systems.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117276</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117276</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - OraTape Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[OraTape Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117056</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117056</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - HeliTape Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[HeliTape Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117053</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117053</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - OraPlug Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[Ora Plug Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117057</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117057</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - INSTAT - Class 2 Recall]]></title>
				<description><![CDATA[INSTAT - Agent, Absorbable Hemostatic, Collagen Based    INSTAT MCH is recommended for use in surgical procedures (other than Urological and Ophthalmological surgery) as an adjunct to hemostatis when control of bleeding by ligature or conventional procedures is ineffective or impractical.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117045</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117045</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - BioMend Absorbable Collagen Membrane - Class 2 Recall]]></title>
				<description><![CDATA[BioMend Absorbable Collagen Membrane    BioMend&#xbf; Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117655</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117655</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - Layershield Adhesion Barrier Matrix - Class 2 Recall]]></title>
				<description><![CDATA[Layershield Adhesion Barrier Matrix    Layershield Adhesion Barrier Matrix is an absorbable implant for use as an adhesion barrier for the reduction of peridural fibrosis.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117062</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117062</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - DuraGen Graft Matrix - Class 2 Recall]]></title>
				<description><![CDATA[Dural Graft Matrix     DuraGen&#xbf; Dural Graft Matrix is an absorbable implant for repair of dural defects. DuraGen matrix is an easy to handle, soft, white, pliable, nonfriable, porous collagen matrix. DuraGen matrix is supplied sterile, nonpyrogenic, for single use in double peel packages in a variety of sizes..]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117035</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117035</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - DuraGen Plus Dural Regeneration Matrix - Class 2 Recall]]></title>
				<description><![CDATA[DuraGen Plus Dural Regeneration Matrix    DuraGen Plus Adhesion Barrier Matrix is an absorbable implant for repair and restoration of dural defects and as an adhesion barrier for the reduction of peridural fibrosis. DuraGen Plus matrix is an easy to handle, soft, white pliable, non-friable, porous, collagen matrix. DuraGen Plus matrix is supplied sterile, nonpyrogenic, for single use in double peel packages in a variety of sizes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117040</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117040</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - HeliPlug Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[HeliPlug Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117055</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117055</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - CollaCote Absorbable Collagen Wound Dressing for Dental Surgery - Class 2 Recall]]></title>
				<description><![CDATA[CollaCote Absorbable Collagen Wound Dressing for Dental Surgery    The Absorbable Collagen Wound Dressings for Dental Surgery are intended for use on moist or bleeding oral wounds where a stabilized blood clot can help protect the surface of the wound from further injury. Topical administration of the Absorbable Collagen Wound Dressings directly over the wound effectively controls bleeding usually within two to five minutes.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117049</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117049</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - OraMem Absorbable Collagen Membrane - Class 2 Recall]]></title>
				<description><![CDATA[OraMem Absorbable Collagen Membrane    OraMem&#xbf; Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117058</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117058</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Integra LifeSciences Corporation - NeuraWrap Nerve Protector - Class 2 Recall]]></title>
				<description><![CDATA[NeuraWrap Nerve Protector    NeuraWrap Nerve Protector is indicated for the management of peripheral nerve injuries in which there has been no substantial loss of nerve tissue.]]></description>
				<pubDate>Sat, 11 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117042</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117042</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DePuy Mitek, Inc., a Johnson &amp; Johnson Co. - DePuy Mitek Tissue Liberator Blade Up - Class 2 Recall]]></title>
				<description><![CDATA[DePuy Mitek Tissue Liberator -Blade Up  Catalog Number:  214623    The Reusable Arthroscopy Instruments are reusable, non-powered surgical instruments used during arthroscopic surgery of any joint except the spine.]]></description>
				<pubDate>Fri, 10 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117373</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117373</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Olympus America Inc. - Olympus SurgMaster UES40 electrosurgical unit (UES40) - Class 2 Recall]]></title>
				<description><![CDATA[Olympus SurgMaster UES-40 electrosurgical unit (&quot;UES-40&quot;)    Product Usage:  Designed for use in a medical facility under the supervision of a trained physician. It has been designed for general (open) and endoscopic surgery including urology, gynecology, respiratory and gastroenterology in conjunction with Olympus designed electrosurgical accessories, endoscopes (fiberscopes, videoscopes and rigid scopes) applicable for electrosurgery (cutting and coagulation), light sources and other ancillary equipment.]]></description>
				<pubDate>Thu, 09 May 2013 01:00:13 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117456</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117456</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Cypress Medical Products LLC - MediChoice Umbilical cord clamp - Class 2 Recall]]></title>
				<description><![CDATA[Cypress Medical Products LLC,  MediChoice Umbilical cord clamp, sterile; single use;  Distributed by Owens &amp; Minor, Mechanicsville, VA.  The product is used to clamp the umbilical cord after childbirth.]]></description>
				<pubDate>Thu, 09 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117289</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117289</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Healthcare Diagnostics, Inc. - Siemens Healthcare Diagnostices Inc. MIcroScan MICroSTREP plus Type 1 B1027201 panels. - Class 2 Recall]]></title>
				<description><![CDATA[Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1 B1027-201 panels.    .MICroSTREP panels are designed for use in determining antimicrobial agent susceptibility of aerobic nonenterococcal streptococci (including Streptococcus pneumoniae) and Haemophilus spp.]]></description>
				<pubDate>Thu, 09 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116809</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116809</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Karl Storz Endoscopy America Inc - Karl Storz Photodynamic Diagnosis (PDD) DLight C System, - Class 2 Recall]]></title>
				<description><![CDATA[KARL STORZ Photodynamic Diagnosis (PDD) D-Light C System,  Instruction Manuals:  PDD Telescopes, Tricam SL II, and PDD Camera Heads.    Used as an optional accessory to white light cystoscopy when used in combination with the diagnostic imaging drug Cysview.]]></description>
				<pubDate>Thu, 09 May 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117240</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117240</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Medshape Solutions, INC. - ExoShape Soft Tissue Fastener 12 mm x 30 mm - Class 2 Recall]]></title>
				<description><![CDATA[ExoShape Soft Tissue Fastener 12 mm x 30 mm REF 1101-00-1230.    For use in the fixation of ligaments, tendons or soft tissue grafts to bone.]]></description>
				<pubDate>Thu, 09 May 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117586</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117586</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Baxter Healthcare Corp. - NonDEHP Catheter Extension Set - Class 2 Recall]]></title>
				<description><![CDATA[A) Product Code 2N8220: Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1)  7.7&quot;, Vol. 1.10 mL, Luer Activated Valve for IV Access, Male Luer Lock Adapter, 2) Medium Catheter Stabilization Device, and 3) Foam Tape Strips;     B) Product Code 2N8221: Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1) 7.1&quot;, Vol. 0.85 mL, Injection Site Male Luer Lock Adapter with Retractable Collar, 2) Medium Catheter Stabilization Device, and 3) Foam Tape Strips;     C) Product Code 2N8222: Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1) 8.2&quot;, Vol. 0.57 mL, Luer Activated Valve for IV Access, Male Luer Lock Adapter, 2) Medium Catheter Stabilization Device, and 3) Foam Tape Strips;     D) Product Code 2N8223: Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1) 7.7&quot;, Vol. 0.40 mL, Injection Site Male Luer Lock Adapter, 2) Medium Catheter Stabilization Device, and 3) Foam Tape Strips;    E) Product Code 6N8220: V-LINK Luer Activated Device with VITALSHIELD Protective Coating Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1) 7.6&quot;, Vol. 1.0 mL, Catheter Extension Set, Luer Activated Device with Silver for IV Access, Male Luer Lock Adapter with Retractable Collar, 2) Medium Catheter Stabilization Device, and 3) Foam Tape Strips;     F) Product Code 6N8222: V-LINK Luer Activated Device with VITALSHIELD Protective Coating Non-DEHP Catheter Extension Set Kit, Single use only, includes: 1) 8.2&quot;, Vol. 0.5 mL, Catheter Extension Set, Luer Activated Device with Silver for IV Access, Male Luer Lock Adapter, 2) Medium Catheter Stabilization Device, and 3) Foam Tape Strips    Product Usage:  The IV extension tubing kits are intended to provide users with a  ready to use  set up for the administration and withdrawal of fluids avoiding the need to acquire/assemble components from various manufacturers. The IV extension tubing sets are indicated for use with a vascular access device for administration and withdrawal of fluids.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116808</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116808</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Baxter Healthcare Corp. - NonDEHP Catheter Extension Set - Class 2 Recall]]></title>
				<description><![CDATA[A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set,  4.8&quot;, Vol. 0.6 mL, Male Luer Lock Adapter, Single use only;     B) Product Code 2N1206: Non-DEHP I.V. Catheter Extension Set, 5.7&quot;, Vol. 0.7 mL, Male Luer Lock Adapter with Retractable Collar, Single use only      Product Usage:  These devices are indicated for use with a vascular access device for administration and withdrawal of fluids.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116800</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116800</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Baxter Healthcare Corp. - NonDEHP Catheter Extension Set - Class 2 Recall]]></title>
				<description><![CDATA[A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set,  5.7&quot;, Vol. 0.8 mL, 2 Injection Sites, Male Luer Lock Adapter, Single use only         Product Usage:  This device is indicated for use in blood sampling and the administration of solutions. The InterLink Injection Site feature is intended to eliminate accidental needle sticks when used in conjunction with an InterLink Cannula as part of an I.V. needless access system.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116807</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116807</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Baxter Healthcare Corp. - NonDEHP Catheter Extension Set - Class 2 Recall]]></title>
				<description><![CDATA[A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit, 6.0&quot;, Vol. 1.0 mL, 2 Luer Activated Valves, Male Luer Lock Adapter, Single use only      Product Usage:  The IV extension tubing kits are intended to provide users with a  ready to use  set up for the administration and withdrawal of fluids avoiding the need to acquire/assemble components from various manufacturers. The IV extension tubing sets are indicated for use with a vascular access device for administration and withdrawal of fluids.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116810</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116810</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Symmetry Medical/SSI - Codman(R) Collins Radioparent Sternal Blade Nylon - Class 2 Recall]]></title>
				<description><![CDATA[Codman(R) Collins Radioparent Sternal Blade Nylon,4 3/4&quot; (121 mm) long,  3&quot; (76 mm) wide, 1 1/2&quot; (38 mm) deep, REF 50-8081    sternum retractor]]></description>
				<pubDate>Wed, 08 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117536</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117536</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smiths Medical ASD, Inc. - Wallace SurePro Two Stage Embryo Replacement Catheter for difficult transfer with Stylet - Class 2 Recall]]></title>
				<description><![CDATA[Wallace Sure-Pro&#xbf; Two Stage Embryo Replacement Catheter for difficult transfer with Stylet  PPS623    Sure-Pro&#xbf; Embryo Replacement Catheters are used for the introduction of embryos into the uterine cavity following in vitro fertilization. Sure-Pro Ultra&#xbf; Embryo Replacement Catheters have the added benefit of being visible under ultrasound. These products can be used in either a one- stage or two-stage procedure. In the one-stage procedure, the clinician pushes the inner catheter through the outer sheath and loads the embryo prior to performing the embryo transfer into the uterus. In the two-stage procedure, the clinician places the outer sheath through the cervical canal into the uterus, then loads the embryo in the inner catheter, and advances the inner catheter through the outer sheath to perform the embryo transfer into the uterus.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116829</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116829</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smiths Medical ASD, Inc. - Wallace SurePro Single Stage Embryo Replacement Catheter - Class 2 Recall]]></title>
				<description><![CDATA[Wallace Sure-Pro&#xbf; Single Stage Embryo Replacement Catheter   Product Code: PP623    Sure-Pro&#xbf; Embryo Replacement Catheters are used for the introduction of embryos into the uterine cavity following in vitro fertilization. Sure-Pro Ultra&#xbf; Embryo Replacement Catheters have the added benefit of being visible under ultrasound. These products can be used in either a one- stage or two-stage procedure. In the one-stage procedure, the clinician pushes the inner catheter through the outer sheath and loads the embryo prior to performing the embryo transfer into the uterus. In the two-stage procedure, the clinician places the outer sheath through the cervical canal into the uterus, then loads the embryo in the inner catheter, and advances the inner catheter through the outer sheath to perform the embryo transfer into the uterus.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117190</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117190</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smiths Medical ASD, Inc. - Wallace SurePro Ultra Embryo Replacement Catheter with Obturator - Class 2 Recall]]></title>
				<description><![CDATA[Wallace Sure-Pro Ultra&#xbf; Embryo Replacement Catheter with Obturator  Product Code: PEB623    Sure-Pro&#xbf; Embryo Replacement Catheters are used for the introduction of embryos into the uterine cavity following in vitro fertilization. Sure-Pro Ultra&#xbf; Embryo Replacement Catheters have the added benefit of being visible under ultrasound. These products can be used in either a one- stage or two-stage procedure. In the one-stage procedure, the clinician pushes the inner catheter through the outer sheath and loads the embryo prior to performing the embryo transfer into the uterus. In the two-stage procedure, the clinician places the outer sheath through the cervical canal into the uterus, then loads the embryo in the inner catheter, and advances the inner catheter through the outer sheath to perform the embryo transfer into the uterus.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116826</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116826</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smiths Medical ASD, Inc. - Wallace SurePro/ SurePro Ultra Embryo Replacement Catheters - Class 2 Recall]]></title>
				<description><![CDATA[Wallace Sure-Pro/ Sure-Pro Ultra Embryo Replacement Catheters  (with ultrasound)  Product Code: PE623    Sure-Pro&#xbf; Embryo Replacement Catheters are used for the introduction of embryos into the uterine cavity following in vitro fertilization. Sure-Pro Ultra&#xbf; Embryo Replacement Catheters have the added benefit of being visible under ultrasound. These products can be used in either a one- stage or two-stage procedure. In the one-stage procedure, the clinician pushes the inner catheter through the outer sheath and loads the embryo prior to performing the embryo transfer into the uterus. In the two-stage procedure, the clinician places the outer sheath through the cervical canal into the uterus, then loads the embryo in the inner catheter, and advances the inner catheter through the outer sheath to perform the embryo transfer into the uterus.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116824</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116824</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smiths Medical ASD, Inc. - Wallace SurePro Ultra Embryo Replacement Catheter with Stylet - Class 2 Recall]]></title>
				<description><![CDATA[Wallace Sure-Pro Ultra&#xbf; Embryo Replacement Catheter with Stylet  Product Code:PES623    Sure-Pro&#xbf; Embryo Replacement Catheters are used for the introduction of embryos into the uterine cavity following in vitro fertilization. Sure-Pro Ultra&#xbf; Embryo Replacement Catheters have the added benefit of being visible under ultrasound. These products can be used in either a one- stage or two-stage procedure. In the one-stage procedure, the clinician pushes the inner catheter through the outer sheath and loads the embryo prior to performing the embryo transfer into the uterus. In the two-stage procedure, the clinician places the outer sheath through the cervical canal into the uterus, then loads the embryo in the inner catheter, and advances the inner catheter through the outer sheath to perform the embryo transfer into the uterus.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116827</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116827</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Smiths Medical ASD, Inc. - Wallace SurePro Two Stage Embryo Replacement  Catheter with Obturator - Class 2 Recall]]></title>
				<description><![CDATA[Wallace Sure-Pro&#xbf; Two Stage Embryo Replacement  Catheter with Obturator  PPB623    Sure-Pro&#xbf; Embryo Replacement Catheters are used for the introduction of embryos into the uterine cavity following in vitro fertilization. Sure-Pro Ultra&#xbf; Embryo Replacement Catheters have the added benefit of being visible under ultrasound. These products can be used in either a one- stage or two-stage procedure. In the one-stage procedure, the clinician pushes the inner catheter through the outer sheath and loads the embryo prior to performing the embryo transfer into the uterus. In the two-stage procedure, the clinician places the outer sheath through the cervical canal into the uterus, then loads the embryo in the inner catheter, and advances the inner catheter through the outer sheath to perform the embryo transfer into the uterus.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116828</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116828</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Synthes USA HQ, Inc. - Synthes Radial Head Prosthesis: Trial Radial Head - Class 2 Recall]]></title>
				<description><![CDATA[Synthes Radial Head Prosthesis: Trial Radial Head    Elbow joint prosthesis: Synthes Radial Head Prosthesis System is a two-piece modular system comprised of titanium alloy stem and cobalt chrome components with an integral screw and side-loading application to allow in-situ assembly.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117017</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117017</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  2mm X 32cm Regular Tip with 1 Hole, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116779</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116779</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  2mm X 32cm Regular Tip with 2 Hole, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116780</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116780</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  3mm X 32cm Regular Tip, Non-Vented, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116794</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116794</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 24cm Regular Tip, Vented, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116777</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116777</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Regular Tip , Non-Vented, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116776</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116776</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Regular Tip with No Holes, Non-Reflective Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116792</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116792</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  2mm X 34cm Regular Tip with No Hole, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116782</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116782</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Regular Tip, Vented, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116763</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116763</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 28cm Regular Tip, vented, Non-Reflective Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116783</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116783</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  3mm X 32cm Regular Tip, Vented, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116793</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116793</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  10mm X 32cm Pool Suction Tip, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116764</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116764</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Regular Tip, Vented, Metal Finish.      Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116762</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116762</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Hydrodissection Tip, Non-Reflective Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116786</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116786</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Becton Dickinson &amp; Co. - BD ProbeTec Neisseria gonorrhoeae (GC) Qx Amplified DNA Assay Reagent Pack - Class 2 Recall]]></title>
				<description><![CDATA[BD ProbeTec Neisseria gonorrhoeae (GC) Qx Amplified DNA Assay Reagent Pack, REF 441124, contains 12 each Microwells labeled in part ***BD ProbeTec Neisseria gonorrhoeae (GC) Qx Amplified DNA Assay Reagent Pack REF 441124 ***For use with the BD Viper System *** Becton, Dickinson and Company 7 Loveton Circle, Sparks, MD 21152 USA www.bd.com/ds EC REP Benex Limited, Pottery Road, Dun Laoghaire, Co. Dublin, Ireland.     Assay is indicated for use with asymptomatic and symptomatic individuals to aid in the diagnosis of gonococcal urogenital disease.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116151</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116151</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Regular Tip, vented, Non-Reflective Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116784</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116784</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 45cm Regular Tip, vented, Non-Reflective Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116790</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116790</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 45cm Regular Tip, Vented, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116775</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116775</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Tip Hydrodissection Tip, Metal Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116765</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116765</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  10mm X 32cm Regular Tip, vented, Non-Reflective Finish.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116785</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116785</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  Vented Tip, 5mm X 45cm Non-Reflective with 30&#xbf; Downward Bend At Proximal End.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116791</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116791</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Endoscopy - Stryker Irrigator Reusable Tips - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Irrigator Reusable Tips:  5mm X 32cm Aspiration Needle Tip.    Suction irrigator tips aid in cleaning and clearing the operative site during  laparoscopic surgery.]]></description>
				<pubDate>Sat, 04 May 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116778</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116778</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Trophy Sas - CareStream Dental - Class 2 Recall]]></title>
				<description><![CDATA[CareStream Dental Kodak 2100 Intraoral X-ray system    Product Usage:  The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.]]></description>
				<pubDate>Fri, 03 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117229</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117229</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Trophy Sas - CareStream Dental - Class 2 Recall]]></title>
				<description><![CDATA[CareStream Dental Kodak 2200 Intraoral X-ray system    Product Usage:  The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.]]></description>
				<pubDate>Fri, 03 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117230</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117230</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Trophy Sas - CareStream Dental - Class 2 Recall]]></title>
				<description><![CDATA[CareStream Dental CS 2100 X-ray system    Product Usage:  The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.]]></description>
				<pubDate>Fri, 03 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116555</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116555</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Trophy Sas - CareStream Dental - Class 2 Recall]]></title>
				<description><![CDATA[CareStream Dental CS 2200  X-ray system    Product Usage:  The expected usage (intended use) for all of these products is for dental radiographic examination and diagnosis of the teeth, jaw and oral structures.]]></description>
				<pubDate>Fri, 03 May 2013 01:00:12 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116556</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116556</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Encore Medical, Lp - Tibial Insert - Class 2 Recall]]></title>
				<description><![CDATA[3DKnee e+ Tibial Insert. The insert is used along with the other components that comprise the 3DKnee System.]]></description>
				<pubDate>Fri, 03 May 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117199</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117199</guid>
			</item>
	
	
			<item>
				<title><![CDATA[NxStage Medical, Inc. - NxStage PureFlowB Solution - Class 2 Recall]]></title>
				<description><![CDATA[NxStage PureFlow-B Solution, Model/Catalog Number: RFP-401, packaged in a case     The NxStage PureFLow-B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.]]></description>
				<pubDate>Fri, 03 May 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117126</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117126</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stryker Howmedica Osteonics Corp. - Class 2 Recall]]></title>
				<description><![CDATA[Stryker Howmedica Osteonics Corp.  AxSOS  System Instrument.    The AxSOS Locking Plate System is designed to treat periarticular or intraarticular fractures of the Distal Femur, Proximal Humerus, Proximal Tibia, and the Distal Tibia. Per the operative technique, &quot; A 4.3 mm Drill (REF 702743) is then used to drill the core hole for the locking screw. Using a fluoroscopy, check the correct depth of the drill, and measure the length of the screw. The Drill Sleeve should now be removed, and the correct length 5.0 mm Locking Screw is inserted using the Screwdriver T20 and Screw Holding Sleeve.&quot;]]></description>
				<pubDate>Thu, 02 May 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117479</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117479</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - Optima MR430s MRI Scanner - Class 2 Recall]]></title>
				<description><![CDATA[Optima MR430s MRI Scanner; 5000-0002    is indicated to use as a magnetic resonance imaging device of the leg (excluding the thigh), knee, ankle, foot, elbow, forearm, wrist, and hand.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117262</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117262</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - MSK EXTREME MR SCANNER - Class 2 Recall]]></title>
				<description><![CDATA[MSK EXTREME MR SCANNER, MODEL AA5000    The intended for use as a diagnostic imaging device to produce axial, sagittal, coronal and oblique images of the internal structures of the leg (excluding the thigh), knee, ankle, foot, forearm, elbow, wrist and hand.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117258</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117258</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Owens &amp; Minor Distribution, Inc. - MediChoice Rayon Tipped OB/GYN Applicator - Class 2 Recall]]></title>
				<description><![CDATA[MediChoice&#xbf; Rayon Tipped OB/GYN Applicator, 8 inch, Plastic Shaft, Non-Sterile, Item Numbers WOD5001 and WOD5002.    Product Usage:  Usage:  An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117406</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117406</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - GE 1.5T SIGNA HDe MR SYSTEM - Class 2 Recall]]></title>
				<description><![CDATA[GE Healthcare, GE 1.5T SIGNA HDe MR SYSTEM.    Indicated for use as a diagnostic imaging device.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117398</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117398</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - Discovery MR750, Discovery 450, Optima 450W (with and without GEM), Signa HDx, Signa HDxt, Signa HDi - Class 2 Recall]]></title>
				<description><![CDATA[GE Healthcare, Discovery MR750, Discovery 450, Optima 450W (with and without GEM), Signa HDx, Signa HDxt, Signa HDi, Signa Vibrant.    Indicated for use as a diagnostic imaging device.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117394</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117394</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - Optima MR360/Brivo MR355 (HDsv), GE 0.35T Signa Ovation HD MR System, GE 0.2T Signa Profile HD MR Sy - Class 2 Recall]]></title>
				<description><![CDATA[GE Healthcare, Optima MR360/Brivo MR355 (HDsv), GE 0.35T Signa Ovation HD MR System, GE 0.2T Signa Profile HD MR System.    Indicated for use as a diagnostic imaging device.]]></description>
				<pubDate>Thu, 02 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117400</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117400</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT7 - Class 2 Recall]]></title>
				<description><![CDATA[GE, VCT for Discovery VCT, Discovery RX VCT, and Discovery PET/CT 690, Lightspeed VCT, Discovery CT750HD.    Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission.]]></description>
				<pubDate>Tue, 30 Apr 2013 01:00:19 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117278</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117278</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Discus Dental LLC - SL3 SOFTTISSUE Laser - Class 2 Recall]]></title>
				<description><![CDATA[SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA 90232.    The SL3 is a soft-tissue diode laser intended to be used for dental procedures]]></description>
				<pubDate>Tue, 30 Apr 2013 01:00:13 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116642</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116642</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien LLC - Covidien MediTrace Cadence Pediatric Radiotransparent Defibrillation Electrode - Class 2 Recall]]></title>
				<description><![CDATA[Medi-Trace Cadence Pediatric Radiotransparent Defibrillation Electrode  Product ID: 22550P.    Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.]]></description>
				<pubDate>Tue, 30 Apr 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117215</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117215</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Masimo Corporation - Pulse Oximeter - Class 2 Recall]]></title>
				<description><![CDATA[Rad-8 Pulse Oximeters     The Rad-8 family of pulse oximeters and accessories are indicated for the continuous, noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate (measured by an SpO2 sensor).]]></description>
				<pubDate>Tue, 30 Apr 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117114</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117114</guid>
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			<item>
				<title><![CDATA[Covidien LLC - Covidien MediTrace Cadence Adult Radiotransparent Defibrillation Electrode - Class 2 Recall]]></title>
				<description><![CDATA[Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode  Product ID: 22550R.    Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.]]></description>
				<pubDate>Tue, 30 Apr 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117214</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117214</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips Healthcare Inc. - HeartStart MRx Defibrillator - Class 2 Recall]]></title>
				<description><![CDATA[HeartStart MRx Monitor/Defribillator; Product Codes:  M3536A, M3536J, M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6.      The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation.]]></description>
				<pubDate>Tue, 30 Apr 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117200</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117200</guid>
			</item>
	
	
			<item>
				<title><![CDATA[B. Braun Medical, Inc. - Diacap(R) Ultra Dialysis Fluid Filter - Class 2 Recall]]></title>
				<description><![CDATA[Diacap(R) Ultra Dialysis Fluid Filter, Catalog Number 7107367.    Intended to filter bacteria and endotoxins from dialysis fluid.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116364</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116364</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Siemens Medical Solutions USA,  Inc - Siemens ARTISTE, ONCOR and PRIMUS systems. - Class 2 Recall]]></title>
				<description><![CDATA[Software correction applies to customers who use the RT Therapist  RTT4.2.108 and RT Therapist Connect RTT 4.2.108   on Siemens ARTISTE, ONCOR and PRIMUS systems.    ARTISTE, ONCOR and PRIMUS family of linear accelerators are used to deliver X-ray photon and electron radiation for the therapeutic treatment of cancer.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117486</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117486</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Vital Images, Inc. - Vitrea - Class 2 Recall]]></title>
				<description><![CDATA[Vitrea&#xbf; CT Brain Perfusion made available in various configurations under the names Vitrea, Vitrea fX, VitreaAdvanced and Vitrea Enterprise Suite.    Noninvasive post-processing application designed to evaluate areas of brain perfusion.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117147</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117147</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Advanced Sterilization Products - STERRAD Cyclesure - Class 2 Recall]]></title>
				<description><![CDATA[STERRAD CYCLESURE 24 Biological Indicator (BI)    The STERRAD CYCLESURE 24 Biological Indicator (BI), is intended to be used as a standard method for frequent monitoring of the STERRAD Sterilization System cycles.]]></description>
				<pubDate>Sat, 27 Apr 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117569</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117569</guid>
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			<item>
				<title><![CDATA[DePuy Mitek, Inc., a Johnson &amp; Johnson Co. - ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 - Class 2 Recall]]></title>
				<description><![CDATA[ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC), Catalog Number: 223111.    For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.]]></description>
				<pubDate>Fri, 26 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116832</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116832</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DePuy Mitek, Inc., a Johnson &amp; Johnson Co. - ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 - Class 2 Recall]]></title>
				<description><![CDATA[ORTHOCORD ONE VIOLET AND ONE BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC), Catalog Number:  223113.    For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.]]></description>
				<pubDate>Fri, 26 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116833</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116833</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DePuy Mitek, Inc., a Johnson &amp; Johnson Co. - ORTHOCORD One Violet and One Blue Braided Composite Suture with MO7 Taper Needles - Class 2 Recall]]></title>
				<description><![CDATA[ORTHOCORD One Violet and One Blue Braided Composite Suture with MO-7 Taper Needles, Catalog Number: 223114.    For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.]]></description>
				<pubDate>Fri, 26 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116834</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116834</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DePuy Mitek, Inc., a Johnson &amp; Johnson Co. - ORTHOCORD One Violet and One Blue Braided Composite Suture with OS6 Reverse Cutting Needles - Class 2 Recall]]></title>
				<description><![CDATA[ORTHOCORD One Violet and One Blue Braided Composite Suture with OS-6 Reverse Cutting Needles, Product Code:  223116.    For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.]]></description>
				<pubDate>Fri, 26 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116836</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116836</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DePuy Mitek, Inc., a Johnson &amp; Johnson Co. - ORTHOCORD One Violet and One Blue Braided Composite Suture with MO6 Taper Needles - Class 2 Recall]]></title>
				<description><![CDATA[ORTHOCORD One Violet and One Blue Braided Composite Suture with MO-6 Taper Needles, Product Code:  223115.    For use in general soft tissue approximation, and/or ligation, including orthopedic procedures.]]></description>
				<pubDate>Fri, 26 Apr 2013 01:00:08 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116835</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116835</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Alere San Diego, Inc. - Alere Cholestech LDX hsCRP Test Cassette, - Class 2 Recall]]></title>
				<description><![CDATA[The Alere Cholestech LDX&#xbf; high sensitivity C-Reactive Protein (hsCRP) Test Cassette, Model Number 12-807.       Product Usage:    Immunoassay for the determination of C-Reactive Protein (CRP). The Alere Cholestech LDX&#xbf; high sensitivity C-Reactive Protein (hsCRP) is an in vitro diagnostic test for the quantitative determination of C-reactive protein in whole blood or serum.]]></description>
				<pubDate>Fri, 26 Apr 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116831</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116831</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Beckman Coulter Inc. - AU5800 Clinical Chemistry Analyzer - Class 2 Recall]]></title>
				<description><![CDATA[AU5800 Clinical Chemistry Analyzer    The Beckman Coulter AU5800 Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC) material and other accessories. This system is for in vitro diagnostic use only. Applications include colorimetric, turbidimetric, latex agglutination, homogeneous enzyme immunoassay, and in selective electrode.]]></description>
				<pubDate>Thu, 25 Apr 2013 01:00:17 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116876</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116876</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - Ventri Discovery NM 530c - Class 2 Recall]]></title>
				<description><![CDATA[Ventri Discovery NM 530c, Ventri with Premium Table Discovery NM 530c, models H3000ZW &amp; H3000SA. The system is used to perform nuclear imaging procedures.]]></description>
				<pubDate>Thu, 25 Apr 2013 01:00:13 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116796</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116796</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips And Neusoft Medical Systems Co., Ltd. - NeuViz 16 MultiSlice CT Scanner System - Class 2 Recall]]></title>
				<description><![CDATA[NeuViz 16 Multi-Slice CT Scanner System, Part number (PN): 989605858501, Model:  NeuViz 16.  This is a computed X-ray, Tomography system.    The NeuViz 16 CT Scanner System can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and detector array with multi-slice capability up to 16 slices simultaneously. The acquired X-RAY transmission data is reconstructed by computer into cross-sectional images of the body from the same axial plane taken at different angles. The system is suitable for all patients]]></description>
				<pubDate>Wed, 24 Apr 2013 01:00:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117085</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117085</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Philips And Neusoft Medical Systems Co., Ltd. - NeuViz  Dual series CT  Scanner  System - Class 2 Recall]]></title>
				<description><![CDATA[NeuViz  Dual series CT  Scanner  System, Part number (PN): 989605651321. This is a computed X-ray, Tomography system.    NeuViz Dual Multi-slice CT Scanner System is intended to produce cross-section images of head and body by computer reconstruction of X-ray transmission data taken at different angles.]]></description>
				<pubDate>Wed, 24 Apr 2013 01:00:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117086</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117086</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Varian Medical Systems, Inc. Oncology Systems - Class 2 Recall]]></title>
				<description><![CDATA[Varian brand RPM Respiratory Gating System, RPM Gating v1.7.5 with 3D Option, Model Number: HS2    Product Usage:  The RPM device is to be used to characterize the patient s respiratory motion information to synchronize their operation with the respiratory motion.]]></description>
				<pubDate>Wed, 24 Apr 2013 01:00:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117140</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117140</guid>
			</item>
	
	
			<item>
				<title><![CDATA[GE Healthcare, LLC - Xeleris 2 Processing &amp; Review Workstation - Class 2 Recall]]></title>
				<description><![CDATA[GE Healthcare, Xeleris 2 Processing &amp; Review Workstation.    The display, processing, archiving, and communication of data acquired by Emission Tomography cameras used in diagnostic radiology, including procedures for planar imaging, whole body imaging, tomographic (SPECT) imaging, positron imaging by coincidence, attenuation correction, and anatomical image registration]]></description>
				<pubDate>Wed, 24 Apr 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117103</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117103</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Teleflex Medical - Belly Bag Urine Collection Bag with Hip Belt. - Class 2 Recall]]></title>
				<description><![CDATA[Belly Bag Urine Collection Bag with Hip Belt.    The product is a sterile urine collection device that collects urine by mechanical means when attached to an indwelling Foley or suprapubic catheter.]]></description>
				<pubDate>Tue, 23 Apr 2013 01:00:11 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116842</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116842</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Stellate Systems - Harmonie software versions 5.1 uo to 6.2e : - Class 2 Recall]]></title>
				<description><![CDATA[Harmonie software versions 5.1 uo to 6.2e :  Harmonie-E Long Term Monitoring system (Models HSYS-REC-WD, HSYS-REC-WT; HSYS-REC0LT2; HSYS-REC-EAMP)    Product in use with Harmonie-E Long Term Monitoring System : ICTA-S &amp; ICTA-D Seizure Detector, Slow wave Seizure Detector Harmonie-S Sleep System: Rapid Eye Movement Detector, Spindle Detector, Heart Rate Processor, Periodic Leg Movement Detector and Oximetry/Pulse rate Threshold Notification VITA/ICU Neurological Monitoring System: Burst Suppression Detector, Cerebral Function Monitor Trend, Visual and Auditory Notifications on all trends graphs in PolyTrends Harmonie {-s}{-E} Readers ,]]></description>
				<pubDate>Tue, 23 Apr 2013 01:00:10 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116691</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116691</guid>
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			<item>
				<title><![CDATA[Spinal Solutions, LLC - APLIF Implants and Instruments - Class 2 Recall]]></title>
				<description><![CDATA[APLIF Implants and Instruments,   Part Numbers:    184008-10 Anterior Psoas Lumbar 18 x 40 x 08mm - 10degree  184010-10 Anterior Psoas Lumbar 18 x 40 x 10mm - 10degree  184012-10 Anterior Psoas Lumbar 18 x 40 x 12mm - 10degree  184014-10 Anterior Psoas Lumbar 18 x 40 x 14mm - 10degree  184016-10 Anterior Psoas Lumbar 18 x 40 x 16mm - 10degree  184008-00 Anterior Psoas Lumbar 18 x 40 x 08mm - 00degree  184010-00 Anterior Psoas Lumbar 18 x 40 x 10mm - 00degree  184012-00 Anterior Psoas Lumbar 18 x 40 x 12mm - 00degree  184014-00 Anterior Psoas Lumbar 18 x 40 x 14mm - 00degree  184016-00 Anterior Psoas Lumbar 18 x 40 x 16mm - 00degree  184510-08 Anterior Psoas Lumbar 18 x 45 x 08mm - 10degree  184510-10 Anterior Psoas Lumbar 18 x 45 x 10mm - 10degree  184512-10 Anterior Psoas Lumbar 18 x 45 x 12mm - 10degree  184514-10 Anterior Psoas Lumbar 18 x 45 x 14mm - 10degree  184516-10 Anterior Psoas Lumbar 18 x 45 x 16mm - 10degree  184510-00 Anterior Psoas Lumbar 18 x 45 x 10mm - 00degree  184512-00 Anterior Psoas Lumbar 18 x 45 x 12mm - 00degree  184514-00 Anterior Psoas Lumbar 18 x 45 x 14mm - 00degree  184516-00 Anterior Psoas Lumbar 18 x 45 x 16mm - 00degree  185008-10 Anterior Psoas Lumbar 18 x 50 x 08mm - 10degree  185010-10 Anterior Psoas Lumbar 18 x 50 x 10mm - 10degree  185012-10 Anterior Psoas Lumbar 18 x 50 x 12mm - 10degree  185014-10 Anterior Psoas Lumbar 18 x 50 x 14mm - 10degree  185016-10 Anterior Psoas Lumbar 18 x 50 x 16mm - 10degree  185008-00 Anterior Psoas Lumbar 18 x 50 x 08mm - 00degree  185010-00 Anterior Psoas Lumbar 18 x 50 x 10mm - 00degree  185012-00 Anterior Psoas Lumbar 18 x 50 x 12mm - 00degree  185014-00 Anterior Psoas Lumbar 18 x 50 x 14mm - 00degree  185016-00 Anterior Psoas Lumbar 18 x 50 x 16mm - 00degree  185508-10 Anterior Psoas Lumbar 18 x 55 x 08mm - 10degree  185510-10 Anterior Psoas Lumbar 18 x 55 x 10mm - 10degree  185512-10 Anterior Psoas Lumbar 18 x 55 x 12mm - 10degree  185514-10 Anterior Psoas Lumbar 18 x 55 x 14mm - 10degree  185516-10 Anterior Psoas Lumbar 18 x 55 x 16mm - 10degree  185508-00 Anterior Psoas Lumbar 18 x 55 x 08mm - 00degree  185510-00 Anterior Psoas Lumbar 18 x 55 x 10mm - 00degree  185512-00 Anterior Psoas Lumbar 18 x 55 x 12mm - 00degree  185514-00 Anterior Psoas Lumbar 18 x 55 x 14mm - 00degree  185516-00 Anterior Psoas Lumbar 18 x 55 x 16mm - 00degree    The Eminent Spine Interbody Fusion System is indicated for intervertebral body fusion of the lumbar spine, from L2 to S1, in skeletally mature patients who have had six months of non-operative treatment.]]></description>
				<pubDate>Tue, 23 Apr 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116518</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116518</guid>
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			<item>
				<title><![CDATA[Orthopedic Alliance LLC - Orthopedic Alliance Spine System (alias Blue &amp; Gold) - Class 2 Recall]]></title>
				<description><![CDATA[Orthopedic Alliance Spine System (alias &quot;Blue &amp; Gold&quot;)    Part Numbers:    BGC3010 Screw Cap  BGR0040 Straight Rod 5.5 x 40mm  BGR0050 Straight Rod 5.5 x 50mm  BGR0060 Straight Rod 5.5 x 60mm  BGR0070 Straight Rod 5.5 x 70mm  BGR0080 Straight Rod 5.5 x 80mm  BGR0090 Straight Rod 5.5 x 90mm  BGR0100 Straight Rod 5.5 x 100mm  BGR0110 Straight Rod 5.5 x 110mm  BGR0120 Straight Rod 5.5 x 120mm  BGR0130 Straight Rod 5.5 x 130mm  BGR0140 Straight Rod 5.5 x 140mm  BGR0150 Straight Rod 5.5 x 150mm  BGR0200 Straight Rod 5.5 x 200mm  BGR0300 Straight Rod 5.5 x 300mm  BGR0400 Straight Rod 5.5 x 400mm  BGR0500 Straight Rod 5.5 x 500mm  BGS5535 5.5 x 35mm Polyaxial Screw  BGS5540 5.5 x 40mm Polyaxial Screw  BGS5545 5.5 x 45mm Polyaxial Screw  BGS6035 6.0 x 35mm Polyaxial Screw  BGS6040 6.0 x 40mm Polyaxial Screw  BGS6045 6.0 x 45mm Polyaxial Screw  BGS6050 6.0 x 50mm Polyaxial Screw  BGS6535 6.5 x 35mm Polyaxial Screw  BGS6540 6.5 x 40mm Polyaxial Screw  BGS6545 6.5 x 45mm Polyaxial Screw  BGS6550 6.5 x 50mm Polyaxial Screw  BGS7035 7.0 x 35mm Polyaxial Screw  BGS7040 7.0 x 40mm Polyaxial Screw  BGS7045 7.0 x 45mm Polyaxial Screw  BGS7050 7.0 x 50mm Polyaxial Screw  BGS7055 7.0 x 55mm Polyaxial Screw  BGS7535 7.5 x 35mm Polyaxial Screw  BGS7540 7.5 x 40mm Polyaxial Screw  BGS7545 7.5 x 45mm Polyaxial Screw    A pedicle screw system intended to provide immobilization and stabilization of spinal segments in skeletally mature patients.]]></description>
				<pubDate>Tue, 23 Apr 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116550</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116550</guid>
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			<item>
				<title><![CDATA[Accuray Incorporated - RoboCouch Patient Positioning System - Class 2 Recall]]></title>
				<description><![CDATA[RoboCouch Patient Positioning System      Product Usage:  is intended for use in the support and positioning of a patient during radiosurgery and radiotherapy procedures and other medical procedures when precise positioning is required.]]></description>
				<pubDate>Sun, 21 Apr 2013 01:00:06 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117112</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117112</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Nova Biomedical Corporation - Nova StatStrip Glucose Test Strips - Class 2 Recall]]></title>
				<description><![CDATA[Nova StatStrip Xpress Glu-Test Strips (Glucose test strips)  Catalog # 51493 (UK Only)]]></description>
				<pubDate>Sat, 20 Apr 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116761</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116761</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Ortho-Clinical Diagnostics - VITROS Chemistry Products PHBR Slides - Class 2 Recall]]></title>
				<description><![CDATA[VITROS Chemistry Products PHBR (Phenobarbital) Slides, REF 822 1384.    For the quantitative measure of phenobarbital (PHBR) concentration in serum and plasma.]]></description>
				<pubDate>Sat, 20 Apr 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116830</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116830</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Nova Biomedical Corporation - Nova StatStrip Glucose Test Strips - Class 2 Recall]]></title>
				<description><![CDATA[Nova StatStrip Xpress Glu-Test Strips (Glucose test strips)  Catalog # 42214]]></description>
				<pubDate>Sat, 20 Apr 2013 01:00:09 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116692</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116692</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Ortho-Clinical Diagnostics - VITROS CKMB Calibrators - Class 3 Recall]]></title>
				<description><![CDATA[VITROS Immunodiagnostic Products CK-MB Calibrators, REF 128 6293, IVD,  Ortho-Clinical Diagnostics High Wycombe HP12 4DP, UK     For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System for the quantitative measurement of CK-MB in human serum and plasma (EDTA or heparin).]]></description>
				<pubDate>Sat, 18 May 2013 01:00:15 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117358</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117358</guid>
			</item>
	
	
			<item>
				<title><![CDATA[DePuy Orthopaedics, Inc. - LifeLiner - Class 3 Recall]]></title>
				<description><![CDATA[DePuy LifeLiner Stick &amp; Cut Resistant Gloves Rt, Lg  Part No. 5200-68-000    The gloves are designed to resist sticks and cuts and are not cut or puncture proof. These gloves are not required by any surgical technique.]]></description>
				<pubDate>Fri, 17 May 2013 01:00:16 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117845</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117845</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Bio-rad Laboratories, Inc. - Liquichek ToRCH Plus IgM Control - Class 3 Recall]]></title>
				<description><![CDATA[Liquichek&quot; ToRCH Plus IgM Control - Positive    Liquichek ToRCH Plus IgM Control is intended for use as an unassayed quality control serum to monitor precision of IgM laboratory testing procedures for the analytes listed in this package insert. This product is not intended for use in blood donor screening assays. Analytes claimed with this lot of Liquichek ToRCH Plus IgM Control: &#xbf; Cytomegalovirus (CMV) IgM &#xbf; Herpes Simplex Virus Type 1/2 (HSV-1/2) IgM &#xbf; Rubella Virus IgM &#xbf; Toxoplasma gondii IgM]]></description>
				<pubDate>Fri, 17 May 2013 01:00:13 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117531</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117531</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien LLC - IV Start Kit - Class 3 Recall]]></title>
				<description><![CDATA[Curity I.V. Start Kit, Product ID: 80530 and Curity I.V. Start Kit Product ID: 8508.    IV Start Kit.]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117368</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117368</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Covidien LLC - Staple Remover Kit - Class 3 Recall]]></title>
				<description><![CDATA[Curity Staple Remover Kit; Product Code: 66701.    Staple Remover Kit.]]></description>
				<pubDate>Sun, 12 May 2013 01:00:05 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117371</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=117371</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 80 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 80 MM Lordosed Rod,  Part Number: 60100-080.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85610</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85610</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 40 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 40 MM Lordosed Rod,   Part Number: 60100-040.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85606</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85606</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 110mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 110mm Straight Rod,  Part Number: 60101-110.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85623</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85623</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 30mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 30mm Straight Rod,  Part Number: 60101-030.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85615</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85615</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 50mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 50mm Straight Rod,  Part Number: 60101-050.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85617</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85617</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 120mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 120mm Straight Rod,  Part Number: 60101-120.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85624</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85624</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 70 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 70 MM Lordosed Rod,  Part Number: 60100-070.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85609</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85609</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 120mm Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 120mm Lordosed Rod,  Part Number: 60100-120.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85614</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85614</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 400mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 400mm Straight Rod,  Part Number: 60101-400.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85625</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85625</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 60mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 60mm Straight Rod,  Part Number: 60101-060.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85618</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85618</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 110mm Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 110mm Lordosed Rod,  Part Number: 60100-110.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85613</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85613</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 80mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 80mm Straight Rod,  Part Number: 60101-080.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85620</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85620</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 90mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 90mm Straight Rod,  Part Number: 60101-090.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85621</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85621</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 40mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 40mm Straight Rod,  Part Number: 60101-040.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85616</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85616</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 100mm Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 100mm Lordosed Rod,  Part Number: 60100-100.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85612</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85612</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 70mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 70mm Straight Rod,  Part Number: 60101-070.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85619</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85619</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 50 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 50 MM Lordosed Rod,  Part Number: 60100-050.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85607</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85607</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 100mm Straight Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 100mm Straight Rod,  Part Number: 60101-100.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85622</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85622</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 90 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 90 MM Lordosed Rod,  Part Number: 60100-090.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85611</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85611</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 30 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 30 MM Lordosed Rod,   Part Number: 60100-030.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85605</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85605</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Spinal Elements, Inc - Mercury Spinal System DIA 5.5 x 60 MM Lordosed Rod - Class 3 Recall]]></title>
				<description><![CDATA[Mercury Spinal System DIA 5.5 x 60 MM Lordosed Rod,  Part Number: 60100-060.    Intended to provide immobilization and stabilization of the spine in skeletally mature patients.]]></description>
				<pubDate>Wed, 08 May 2013 01:00:07 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85608</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=85608</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Ortho-Clinical Diagnostics - VITROS AntiHBS Reagent Pack - Class 3 Recall]]></title>
				<description><![CDATA[VITROS&#xbf; Immunodiagnostic Products Anti-HBs (total antibody to hepatitis B surface antigen (anti-HBs)) Reagent Packs      For the quantitative in vitro determination of total antibody to hepatitis B surface antigen (anti-HBs) in human serum.]]></description>
				<pubDate>Wed, 24 Apr 2013 01:00:20 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116884</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116884</guid>
			</item>
	
	
			<item>
				<title><![CDATA[Sirtex Medical Limited - Sirtex SIRyttrium 90 microspheres (Radionuclide) - Class 3 Recall]]></title>
				<description><![CDATA[Sirtex SIR-yttrium 90 microspheres (Radionuclide); SIR-Y001.    Indicated for the treatment of unresectable metastatic liver tumors.]]></description>
				<pubDate>Wed, 24 Apr 2013 01:00:14 GMT</pubDate>
				<link>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116369</link>
				<guid>http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=116369</guid>
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