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	<title>NewsInferno &#187; Recalled Medical Devices</title>
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		<title>Synthes USA Issues Class I Recall for Vertebrae Replacement Implants</title>
		<link>http://www.newsinferno.com/archives/13875</link>
		<comments>http://www.newsinferno.com/archives/13875#comments</comments>
		<pubDate>Fri, 13 Nov 2009 17:44:11 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=13875</guid>
		<description><![CDATA[Synthes USA is recalling all lots of the Ti Synex II Vertebral Body Replacement device.   The U.S. Food &#038; Drug Administration (FDA) has deemed the Synthes USA Ti Synex II Vertebral Body Replacement recall a Class I recall.
The Ti Synex II Vertebral Body Replacement is used in the T1-L5 portion of the spine [...]]]></description>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>Edwards Lifesciences Recalls Aortic Catheters</title>
		<link>http://www.newsinferno.com/archives/13828</link>
		<comments>http://www.newsinferno.com/archives/13828#comments</comments>
		<pubDate>Tue, 10 Nov 2009 19:11:21 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=13828</guid>
		<description><![CDATA[Edwards Lifesciences Corporation has issued a recall of CardioVations EndoClamp Aortic Catheter.  The Food &#038; Drug Administration (FDA) has deemed this a Class I recall, its most serious type of recall.  
The CardioVations EndoClamp Aortic Catheter locks off the aorta, monitors aortic pressure, and delivers solution to stop the heart during cardiopulmonary bypass [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Cordis Recalls Crossover Sheath Introducer</title>
		<link>http://www.newsinferno.com/archives/13685</link>
		<comments>http://www.newsinferno.com/archives/13685#comments</comments>
		<pubDate>Mon, 02 Nov 2009 18:29:31 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=13685</guid>
		<description><![CDATA[Cordis Corporation is recalling all lots of the Crossover Sheath Introducer due to complaints about stretching or fracture of the sheath during use.  
To date, Cordis has received six complaints about the Crossover Sheath Introducer.  No permanent patient injuries have been reported. In two instances, successful surgical intervention was performed to retrieve a [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Qualitest Pharmaceuticals Issues Recall For All Accusure® Insulin Syringes</title>
		<link>http://www.newsinferno.com/archives/13612</link>
		<comments>http://www.newsinferno.com/archives/13612#comments</comments>
		<pubDate>Wed, 28 Oct 2009 14:54:17 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=13612</guid>
		<description><![CDATA[A voluntary nationwide recall was issued yesterday for all Accusure® Insulin Syringes manufactured by Qualitest Pharmaceuticals of Huntsville, Alabama.
The recalled syringes may have needles which detach from the syringe. According to the recall notice, if the needle becomes detached from the syringe during use, it can become stuck in the insulin vial, push back into [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Unomedical Recalls Manual Pulmonary Resuscitators</title>
		<link>http://www.newsinferno.com/archives/13276</link>
		<comments>http://www.newsinferno.com/archives/13276#comments</comments>
		<pubDate>Thu, 08 Oct 2009 17:37:41 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=13276</guid>
		<description><![CDATA[Certain units of the single-patient use Manual Pulmonary Resuscitator (MPR) have been recalled by Unomedical Inc.  This recall is being conducted because of a potential malfunction of  the MPR, which may impair the ability of the device to generate the positive pressure necessary to function properly. The occurrence of such a malfunction may [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/13276/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Accu-Check Spirit Insulin Pumps Recalled</title>
		<link>http://www.newsinferno.com/archives/5877</link>
		<comments>http://www.newsinferno.com/archives/5877#comments</comments>
		<pubDate>Fri, 01 May 2009 15:24:29 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=5877</guid>
		<description><![CDATA[Accu-Check Spirit insulin pumps are being recalled by Disetronic Medical Systems Inc., a unit of the Roche Group,  because of a  potential defect in the “up” and/or “down” buttons of some devices.  According to the recall notice, if the buttons do not function, users may not be able to change any programmed [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Medtronic Recalls BioGlide Ventricular Shunt Catheters</title>
		<link>http://www.newsinferno.com/archives/5343</link>
		<comments>http://www.newsinferno.com/archives/5343#comments</comments>
		<pubDate>Mon, 30 Mar 2009 13:53:55 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Products]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=5343</guid>
		<description><![CDATA[A class I recall has been issued for Medtronic BioGlide Ventricular Shunt Catheters.   A class I recall is issued when a device poses a risk of serious injury and death.
The recalled Medtronic BioGlide Ventricular Shunt Catheter is part of a system used to treat a condition called hydrocephalus, which is characterized by an [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Calaxo Bone Screw Causing Painful Complications for ACL Surgery Patients</title>
		<link>http://www.newsinferno.com/archives/5134</link>
		<comments>http://www.newsinferno.com/archives/5134#comments</comments>
		<pubDate>Wed, 18 Mar 2009 15:11:01 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=5134</guid>
		<description><![CDATA[A simple medical device called the Calaxo Bone Screw has been causing a great deal of pain and suffering for those who have undergone Anterior Cruciate Ligament (ACL) reconstructive surgery.  The Calaxo Bone Screw was recalled in August 2007 due to reports of serious complications.  Some patients even had to have repeat surgeries [...]]]></description>
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		<slash:comments>8</slash:comments>
		</item>
		<item>
		<title>Welch Allyn Recalls Automatic External Defibrillators</title>
		<link>http://www.newsinferno.com/archives/5113</link>
		<comments>http://www.newsinferno.com/archives/5113#comments</comments>
		<pubDate>Tue, 17 Mar 2009 13:39:01 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=5113</guid>
		<description><![CDATA[Welch Allyn has issued a worldwide recall of various AED 10 and MRL JumpStart automatic external defibrillators manufactured between October 3, 2002 and January 25, 2007.  The Food &#038; Drug Administration (FDA) has deemed the Welch Allyn defibrillator recall a Class I recall because there is a reasonable probability that use of the product [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Covidien Recalls Pediatric Tracheostomy Tubes</title>
		<link>http://www.newsinferno.com/archives/5018</link>
		<comments>http://www.newsinferno.com/archives/5018#comments</comments>
		<pubDate>Wed, 11 Mar 2009 13:39:50 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/?p=5018</guid>
		<description><![CDATA[Covidien Inc. is recalling several lots of Shiley 3.0PED Cuffless Pediatric Tracheostomy Tubes because practitioners have reported difficulty inserting two of the device&#8217;s components during procedures.  The action has been deemed a Class I recall, the Food &#038; Drug Administration&#8217;s (FDA) most urgent type of  recall.  Class I recalls are issued when [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/5018/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Stryker Recalls Crania Implant Kits</title>
		<link>http://www.newsinferno.com/archives/4432</link>
		<comments>http://www.newsinferno.com/archives/4432#comments</comments>
		<pubDate>Fri, 26 Dec 2008 17:00:53 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/4432</guid>
		<description><![CDATA[Custom-made Cranial Implant Kits made by Stryker Corp. have been recalled over sterility issues.  According to the Food &#038; Drug Administration (FDA), the Cranial Implant Kits are used to correct defects in the jaw and face, or cranium and face.
The Stryker cranial implant kit recall has been deemed a Class I recall by the FDA.  [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/4432/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Sun Med Laryngoscope Blades Named in Class I Recall</title>
		<link>http://www.newsinferno.com/archives/4404</link>
		<comments>http://www.newsinferno.com/archives/4404#comments</comments>
		<pubDate>Mon, 22 Dec 2008 14:15:08 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/4404</guid>
		<description><![CDATA[A Class I recall has been issued for laryngoscope blades distributed by Sun Med of Largo, Florida.  The Food &#038; Drug Administration (FDA) issues Class I recalls when there is a reasonable probability that the use of a device will cause adverse health consequences or death.
The Sun Med laryngoscope recall involves Greenline/D MacIntosh No. 3 [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/4404/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Unapproved Medical Devices Subject to Class I Recall</title>
		<link>http://www.newsinferno.com/archives/4369</link>
		<comments>http://www.newsinferno.com/archives/4369#comments</comments>
		<pubDate>Tue, 16 Dec 2008 14:21:37 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/4369</guid>
		<description><![CDATA[Federal regulators have announced a Class I recall of two unapproved medical devices.  The recall involves Vibrational Integrated Bio-photonic Energizer (VIBE device) sold by VIBE Technologies of Greeley, CO and the HLX8 device marketed by Nebion LLC of Los Angeles, Calif.  According to the agency&#8217;s recall notice, neither VIBE Technologies nor Nebion has demonstrated to [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/4369/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Integra NeuroSciences Recalls Gravity Compensating Accessory</title>
		<link>http://www.newsinferno.com/archives/4357</link>
		<comments>http://www.newsinferno.com/archives/4357#comments</comments>
		<pubDate>Fri, 12 Dec 2008 19:35:47 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/4357</guid>
		<description><![CDATA[Integra NeuroSciences is recalling Gravity Compensating Accessories used with brain shunting systems.  According to the Food &#038; Drug Administration (FDA)  notice, the Gravity Compensating Accessory recall is a Class I recall &#8211; the agency&#8217;s most serious type.
A shunt is a tube that is placed in one of the fluid-filled chambers inside the brain. When infection [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/4357/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>AMO Recalls Eye Surgery Syringes</title>
		<link>http://www.newsinferno.com/archives/4353</link>
		<comments>http://www.newsinferno.com/archives/4353#comments</comments>
		<pubDate>Fri, 12 Dec 2008 14:09:17 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/4353</guid>
		<description><![CDATA[Advanced Medical Optics (AMO) has announced a Class I recall of its Healon D Ophthalmic Viscosurgical Device (OVD) because of a contamination issue.  According to the Food &#038; Drug Administration (FDA), some physicians who used a Healon D OVD during eye surgery observed an inflammatory reaction in their patients at the one-day post-operative visit.
The AMO [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/4353/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>ReliOn Insulin Syringes Sold at Wal-Mart, Sam&#8217;s Clubs Recalled</title>
		<link>http://www.newsinferno.com/archives/4142</link>
		<comments>http://www.newsinferno.com/archives/4142#comments</comments>
		<pubDate>Thu, 06 Nov 2008 14:33:04 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/4142</guid>
		<description><![CDATA[ReliOn Insulin Syringes used by diabetics have been recalled by Tyco Healthcare Group LP (Covidien).   The Food &#038; Drug Administration (FDA) said the syringes may lead to patients receiving an overdose of as much as 2.5 times the intended dose, which may lead to hypoglycemia, serious health consequences, and even death.
The recall involves one lot [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/4142/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Medtronic Drug Pump Catheter Alert Now a Class I Recall</title>
		<link>http://www.newsinferno.com/archives/3910</link>
		<comments>http://www.newsinferno.com/archives/3910#comments</comments>
		<pubDate>Mon, 29 Sep 2008 13:49:42 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/3910</guid>
		<description><![CDATA[A defective Medtronic catheter used in the company’s implantable intrathecal pain pumps has been linked to the death of one patient.  In June, the company alerted doctors to the problem, but now, the Food &#038; Drug Administration (FDA) has classified  Medtronic’s catheter safety alert a Class I recall.  Such a recall is defined as a [...]]]></description>
		<wfw:commentRss>http://www.newsinferno.com/archives/3910/feed</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Sage Products  Recalls Medical Device for Bacterial Contamination</title>
		<link>http://www.newsinferno.com/archives/3372</link>
		<comments>http://www.newsinferno.com/archives/3372#comments</comments>
		<pubDate>Tue, 01 Jul 2008 13:48:26 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/3372</guid>
		<description><![CDATA[Sage Products Inc. has issued a recall of  some lots of 2% Chlorhexidine Gluconate Cloth Patient Preoperative Skin Preparation because it could be contaminated with the bacteria Burkholderia cepacia (B. cepacia). Customers who have these products should stop usage, sale and distribution, and should contact Sage Products to coordinate product return and replacement.
According to [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Ford Owners Warned Again on Defective Cruise Control Switch</title>
		<link>http://www.newsinferno.com/archives/2656</link>
		<comments>http://www.newsinferno.com/archives/2656#comments</comments>
		<pubDate>Fri, 29 Feb 2008 18:07:31 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/2656</guid>
		<description><![CDATA[Faulty Ford cruise control switches are the subject of yet another consumer safety warning.  Thursday, the government warned owners of about 4.6 million recalled Ford vehicles to bring their cars and trucks in immediately to dealerships to disconnect the cruise control switch systems because they have been linked to engine fires.  The National Highway Traffic [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Sierra Pre-Filled Syringe Debacle Yields Five More Lawsuits</title>
		<link>http://www.newsinferno.com/archives/2458</link>
		<comments>http://www.newsinferno.com/archives/2458#comments</comments>
		<pubDate>Fri, 25 Jan 2008 21:59:48 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

		<guid isPermaLink="false">http://www.newsinferno.com/archives/2458</guid>
		<description><![CDATA[Sierra Pre-Filled bacteria tainted syringes continue to be the target of lawsuits.  Five people filed a lawsuit Thursday against Sierra Pre-Filled of Angier, North Carolina, manufacturer of the contaminated pre-filled syringes.  All five claimants are Illinois residents and patients at Rush University Medical Center in Chicago.  The five Sierra Pre-Filled syringe lawsuit [...]]]></description>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Johnson &amp; Johnson Cordis Balloon Catheters Recalled for Potentially Fatal Flaw</title>
		<link>http://www.newsinferno.com/archives/2457</link>
		<comments>http://www.newsinferno.com/archives/2457#comments</comments>
		<pubDate>Fri, 25 Jan 2008 21:35:05 +0000</pubDate>
		<dc:creator>Laurie</dc:creator>
				<category><![CDATA[Defective Medical Devices]]></category>
		<category><![CDATA[Legal News]]></category>
		<category><![CDATA[Product Recalls]]></category>
		<category><![CDATA[Recalled Medical Devices]]></category>

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		<description><![CDATA[Johnson &#038; Johnson has recalled balloon catheters used in angioplasties following reports that the defective medical devices injured two people.  The Fire Star-RX and Dura Star-RX PTCA balloon catheters, which are manufactured by Johnson &#038; Johnson’s Cordis unit, do not deflate properly and could potentially cause  fatal injuries.  For that reason, the Food &#038; Drug [...]]]></description>
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