<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>US Recall News &#187; FDA Press Releases</title>
	<atom:link href="http://www.usrecallnews.com/section/drug-recalls/fda-pr/feed" rel="self" type="application/rss+xml" />
	<link>http://www.usrecallnews.com</link>
	<description>Your one-stop-shop for information on recalled consumer products, pharmaceutical drugs alerts, health supplements recalls, recalled vehicles, automotive parts, boats and more.</description>
	<lastBuildDate>Thu, 05 Nov 2009 03:42:40 +0000</lastBuildDate>
	<generator>http://wordpress.org/?v=2.8.5</generator>
	<language>en</language>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>1</sy:updateFrequency>
			<item>
		<title>BODYBUILDING.COM Conductings International Recall of 65 Dietary Supplements That May Contain Steroids</title>
		<link>http://www.usrecallnews.com/2009/11/fda-7480.html</link>
		<comments>http://www.usrecallnews.com/2009/11/fda-7480.html#comments</comments>
		<pubDate>Wed, 04 Nov 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[bodybuilding]]></category>
		<category><![CDATA[steroids]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/11/fda-7480.html</guid>
		<description><![CDATA[BODYBUILDING.COM Is Conducting a Voluntary Nationwide and International Recall of 65 Dietary Supplements That May Contain Steroids<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/11/fda-7480.html">BODYBUILDING.COM Conductings International Recall of 65 Dietary Supplements That May Contain Steroids</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/11/fda-7480.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Pointe Scientific Expands Recall of Liquid Glucose Hexokinase Reagent (G7517)</title>
		<link>http://www.usrecallnews.com/2009/11/fda-7469.html</link>
		<comments>http://www.usrecallnews.com/2009/11/fda-7469.html#comments</comments>
		<pubDate>Sun, 01 Nov 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Kexokinase]]></category>
		<category><![CDATA[liquid glucose]]></category>
		<category><![CDATA[Pointe Scientific]]></category>
		<category><![CDATA[Reagent]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/11/fda-7469.html</guid>
		<description><![CDATA[Pointe Scientific is recalling all size kits of Liquid Glucose Hexokinase Reagent catalog number G7517.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/11/fda-7469.html">Pointe Scientific Expands Recall of Liquid Glucose Hexokinase Reagent (G7517)</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/11/fda-7469.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Cordis Recalls Crpsspver Sheath Introducer</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7416.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7416.html#comments</comments>
		<pubDate>Sat, 31 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Cordis]]></category>
		<category><![CDATA[cross over]]></category>
		<category><![CDATA[crossover sheath introducer]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7416.html</guid>
		<description><![CDATA[Cordis Corporation announced today a nationwide voluntary recall of all lots of the CROSSOVER™ Sheath Introducer due to complaints about stretching or fracture of the sheath during use. 
The CROSSOVER Sheath Introducer is a product developed and manufactured by Thomas Medical Products, Inc., and distributed by Cordis.  It is a long-coil reinforced, kink-resistant catheter [...]<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7416.html">Cordis Recalls Crpsspver Sheath Introducer</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7416.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Pointe Scientific Recalls Liquid Glucose Hexokinase Reagent (G7517)</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7417.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7417.html#comments</comments>
		<pubDate>Sat, 31 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Kexokinase]]></category>
		<category><![CDATA[liquid glucose]]></category>
		<category><![CDATA[Reagent]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7417.html</guid>
		<description><![CDATA[Product involved in the recall can be identified by any of the lot numbers listed above appearing on the Pointe Scientific, Inc kit content label, vial label or bulk container label.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7417.html">Pointe Scientific Recalls Liquid Glucose Hexokinase Reagent (G7517)</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7417.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Qualitest Pharmaceuticals Issues a Voluntary Nationwide Recall of All AccusureÂ® Insulin Syringes</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7403.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7403.html#comments</comments>
		<pubDate>Wed, 28 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Qualitest Pharmaceuticals]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7403.html</guid>
		<description><![CDATA[If the needle becomes detached from the syringe during use, it can become stuck in the insulin vial, push back into to the syringe, or remain in the skin after injection.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7403.html">Qualitest Pharmaceuticals Issues a Voluntary Nationwide Recall of All AccusureÂ® Insulin Syringes</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7403.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>San Link Inc. Issues an Alert on Uneviscerated Vacuum Pack Dried Krasnoperka (Fish).</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7405.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7405.html#comments</comments>
		<pubDate>Wed, 28 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7405.html</guid>
		<description><![CDATA[

Stay up to date on: product recalls.San Link Inc. Issues an Alert on Uneviscerated Vacuum Pack Dried Krasnoperka (Fish).
<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7405.html">San Link Inc. Issues an Alert on Uneviscerated Vacuum Pack Dried Krasnoperka (Fish).</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7405.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>American Regent Recalls All Lots of Ketorolac Tromethamine Injection</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7353.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7353.html#comments</comments>
		<pubDate>Thu, 22 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[American Regent]]></category>
		<category><![CDATA[Ketorolac Tromethamine Injection]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7353.html</guid>
		<description><![CDATA[American Regent conducts nationwide voluntary recall of ALL lots of its Ketorolac Tromethamine Injection, USP 30 mg/mL.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7353.html">American Regent Recalls All Lots of Ketorolac Tromethamine Injection</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7353.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Unomedical Issues Worldwide Recall of Certain Manual Pulmonary Resuscitators</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7221.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7221.html#comments</comments>
		<pubDate>Thu, 08 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[MPR units]]></category>
		<category><![CDATA[unomedical devices]]></category>
		<category><![CDATA[worldwide]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7221.html</guid>
		<description><![CDATA[The MPR is a single-patient use device used by healthcare professionals. It is intended for patients requiring total or intermittent ventilatory support.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7221.html">Unomedical Issues Worldwide Recall of Certain Manual Pulmonary Resuscitators</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7221.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Neuron 6F 070 Delivery Catheter &#8211; Penumbra</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7222.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7222.html#comments</comments>
		<pubDate>Thu, 08 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[neuron delivery catheter]]></category>
		<category><![CDATA[penumbra]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7222.html</guid>
		<description><![CDATA[Facilities that have the older version of 6F Neuron 070 Delivery Catheter which is being recalled should stop using and return the device.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7222.html">Neuron 6F 070 Delivery Catheter &#8211; Penumbra</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7222.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Philips Recalls Select Heartstart Fr2+ Automated External Defibrillators</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7188.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7188.html#comments</comments>
		<pubDate>Sun, 04 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[aed]]></category>
		<category><![CDATA[AEDs]]></category>
		<category><![CDATA[external defibrillators]]></category>
		<category><![CDATA[FR2+]]></category>
		<category><![CDATA[heart start]]></category>
		<category><![CDATA[heartstart]]></category>
		<category><![CDATA[Philips]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7188.html</guid>
		<description><![CDATA[Philips is voluntarily recalling approximately 5,400 HeartStart FR2+ automated external defibrillators (AEDs).<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7188.html">Philips Recalls Select Heartstart Fr2+ Automated External Defibrillators</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7188.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>FDA Alert: New USP Standards for Heparin Products Will Result in Decreased Potency</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7158.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7158.html#comments</comments>
		<pubDate>Fri, 02 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[dose]]></category>
		<category><![CDATA[dosing]]></category>
		<category><![CDATA[fda]]></category>
		<category><![CDATA[heparine]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7158.html</guid>
		<description><![CDATA[Healthcare providers should be aware of the potency change for heparin products and the possible clinical effects of this decrease in potency per USP unit dose.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7158.html">FDA Alert: New USP Standards for Heparin Products Will Result in Decreased Potency</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7158.html/feed</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Penumbra Recalls the Original Version of 6F Neuron 070 Delivery Catheter</title>
		<link>http://www.usrecallnews.com/2009/10/fda-7155.html</link>
		<comments>http://www.usrecallnews.com/2009/10/fda-7155.html#comments</comments>
		<pubDate>Thu, 01 Oct 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Urgent Recalls]]></category>
		<category><![CDATA[6F Neuron 070]]></category>
		<category><![CDATA[Delivery Catheter]]></category>
		<category><![CDATA[penumbra]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/10/fda-7155.html</guid>
		<description><![CDATA[Penumbra voluntarily conducted a field removal of the devices after learning about the devices potential to kink or ovalize. FDA has been apprised of this action.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/10/fda-7155.html">Penumbra Recalls the Original Version of 6F Neuron 070 Delivery Catheter</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/fda-7155.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Nationwide Recall of Neocate Infant Specialized Formula Lot P91877</title>
		<link>http://www.usrecallnews.com/2009/09/fda-7134.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-7134.html#comments</comments>
		<pubDate>Tue, 29 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[infant formula]]></category>
		<category><![CDATA[Neocate]]></category>
		<category><![CDATA[specialized]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-7134.html</guid>
		<description><![CDATA[NuNutricia has recalled one lot of the specialized infant formula product, Neocate. This recall involves a limited quantity of individual cans from Lot # P91877.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-7134.html">Nationwide Recall of Neocate Infant Specialized Formula Lot P91877</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-7134.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Portex Uncuffed Pediatric-Sized Tracheal Tubes</title>
		<link>http://www.usrecallnews.com/2009/09/fda-7034.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-7034.html#comments</comments>
		<pubDate>Tue, 22 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[pediatric]]></category>
		<category><![CDATA[Portex]]></category>
		<category><![CDATA[Tracheal Tubes]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-7034.html</guid>
		<description><![CDATA[Smiths Medical announced that it is initiating a nationwide voluntary recall of Portex Uncuffed Pediatric-Sized Tracheal Tubes manufactured before September 2009.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-7034.html">Portex Uncuffed Pediatric-Sized Tracheal Tubes</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-7034.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>FDA Warning: Do Not Use Stolen Albuterol Sulfate and Ipratropium Bromide Inhalation Solutions</title>
		<link>http://www.usrecallnews.com/2009/09/fda-6987.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-6987.html#comments</comments>
		<pubDate>Fri, 18 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Inhalation Solution]]></category>
		<category><![CDATA[Ipratropium Bromide]]></category>
		<category><![CDATA[Stolen Albuterol Sulfate]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-6987.html</guid>
		<description><![CDATA[The U.S. Food and Drug Administration advised consumers not to use certain respiratory medications purchased after Sept. 8, 2009 and manufactured by Dey L.P., a subsidiary of Mylan Inc., because the medications might have been part of a shipment being transported on a tractor-trailer stolen in Tampa, Fla., on Sept. 8, 2009.
The respiratory medications, Ipratropium [...]<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-6987.html">FDA Warning: Do Not Use Stolen Albuterol Sulfate and Ipratropium Bromide Inhalation Solutions</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-6987.html/feed</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>LIFEPAK CR Plus Automated External Defibrillators</title>
		<link>http://www.usrecallnews.com/2009/09/fda-6976.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-6976.html#comments</comments>
		<pubDate>Thu, 17 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[aed]]></category>
		<category><![CDATA[automated external defibrillators]]></category>
		<category><![CDATA[CR Plus]]></category>
		<category><![CDATA[Lifepak]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-6976.html</guid>
		<description><![CDATA[An extremely humid environment may cause the affected devices to improperly analyze the heart rhythm and may cause the device to delay or fail to deliver therapy.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-6976.html">LIFEPAK CR Plus Automated External Defibrillators</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-6976.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>FDA Requires Boxed Warning for Promethazine Hydrochloride Injection</title>
		<link>http://www.usrecallnews.com/2009/09/fda-6977.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-6977.html#comments</comments>
		<pubDate>Thu, 17 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[hydrochloride injection]]></category>
		<category><![CDATA[promethazine]]></category>
		<category><![CDATA[Wyeth pharmaceuticals]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-6977.html</guid>
		<description><![CDATA[Promethazine was previously sold under the brand name Phenergan, but that formulation was discontinued by Wyeth Pharmaceuticals Inc. A number of companies currently market generic formulations of promethazine hydrochloride injection.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-6977.html">FDA Requires Boxed Warning for Promethazine Hydrochloride Injection</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-6977.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Arbonne International, LLC Recalls One Lot of Seasource Detox Spa Foaming Sea Salt Scrub</title>
		<link>http://www.usrecallnews.com/2009/09/fda-6935.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-6935.html#comments</comments>
		<pubDate>Sat, 12 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Foaming Sea Salt Scrub]]></category>
		<category><![CDATA[Seasource Detox Spa]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-6935.html</guid>
		<description><![CDATA[This voluntary recall was initiated by Arbonne as a result of discovering the presence of Pseudomonas aeruginosa bacteria in the recalled lot.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-6935.html">Arbonne International, LLC Recalls One Lot of Seasource Detox Spa Foaming Sea Salt Scrub</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-6935.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Smiths Medical Issues Urgent Device Recall Of Portex Pediatric-Sized Tracheal Tubes</title>
		<link>http://www.usrecallnews.com/2009/09/fda-6936.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-6936.html#comments</comments>
		<pubDate>Sat, 12 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[Pediatric-Sized]]></category>
		<category><![CDATA[Portex]]></category>
		<category><![CDATA[Tracheal Tubes]]></category>
		<category><![CDATA[[edoactrocs]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-6936.html</guid>
		<description><![CDATA[A small number of tubes were manufactured with internal diameters slightly smaller than indicated on the labeling, which may create the potential for the clinician to experience difficulty passing through or withdrawing the suction catheter.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-6936.html">Smiths Medical Issues Urgent Device Recall Of Portex Pediatric-Sized Tracheal Tubes</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-6936.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>CONMED Corporation Recalls Certain Powered Surgical Instrument Products</title>
		<link>http://www.usrecallnews.com/2009/09/fda-6938.html</link>
		<comments>http://www.usrecallnews.com/2009/09/fda-6938.html#comments</comments>
		<pubDate>Sat, 12 Sep 2009 00:00:00 +0000</pubDate>
		<dc:creator>FDA</dc:creator>
				<category><![CDATA[FDA Press Releases]]></category>
		<category><![CDATA[conmed]]></category>
		<category><![CDATA[handpieces]]></category>
		<category><![CDATA[linvatec]]></category>
		<category><![CDATA[pro5]]></category>
		<category><![CDATA[pro6]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/2009/09/fda-6938.html</guid>
		<description><![CDATA[In the PRO5 and PRO6 Medical Device Safety Alert Letter, CONMED Linvatec notified customers about the unlikely possibility for units to potentially self-activate.<p>Stay up to date on: <a href="http://www.usrecallnews.com">product recalls</a>.<br/><br/><a href="http://www.usrecallnews.com/2009/09/fda-6938.html">CONMED Corporation Recalls Certain Powered Surgical Instrument Products</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/fda-6938.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
	</channel>
</rss>

<!-- Dynamic Page Served (once) in 0.770 seconds -->
