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<channel>
	<title>US Recall News &#187; Drug Recalls</title>
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	<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>
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			<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>
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		<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>Decreased Sex Drive in Men: Is Your Low Libido Just Normal?</title>
		<link>http://www.usrecallnews.com/2009/10/decreased-sex-drive-in-men-is-your-low-libido-just-normal.html</link>
		<comments>http://www.usrecallnews.com/2009/10/decreased-sex-drive-in-men-is-your-low-libido-just-normal.html#comments</comments>
		<pubDate>Sun, 04 Oct 2009 18:47:20 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[andropaus]]></category>
		<category><![CDATA[low libido]]></category>
		<category><![CDATA[low sex drive]]></category>
		<category><![CDATA[male menopause]]></category>
		<category><![CDATA[man]]></category>
		<category><![CDATA[manopause]]></category>
		<category><![CDATA[men]]></category>
		<category><![CDATA[testosterone]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7189</guid>
		<description><![CDATA[A decreased sex drive (libido) in men is often a symptom of conditions like low testosterone related to aging, but could also be side effects associated with certain medications.<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/decreased-sex-drive-in-men-is-your-low-libido-just-normal.html">Decreased Sex Drive in Men: Is Your Low Libido Just Normal?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/decreased-sex-drive-in-men-is-your-low-libido-just-normal.html/feed</wfw:commentRss>
		<slash:comments>1</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>Decreased Libido in Women: A Symptom or Side Effect?</title>
		<link>http://www.usrecallnews.com/2009/10/decreased-sex-drive-in-women-a-symptom-or-side-effect.html</link>
		<comments>http://www.usrecallnews.com/2009/10/decreased-sex-drive-in-women-a-symptom-or-side-effect.html#comments</comments>
		<pubDate>Fri, 02 Oct 2009 20:42:22 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[age]]></category>
		<category><![CDATA[decreased sex drive]]></category>
		<category><![CDATA[Dyspareunia]]></category>
		<category><![CDATA[fibromyalgia]]></category>
		<category><![CDATA[hormonal imbalance]]></category>
		<category><![CDATA[hormone]]></category>
		<category><![CDATA[Lexapro]]></category>
		<category><![CDATA[low libido]]></category>
		<category><![CDATA[side effects]]></category>
		<category><![CDATA[symptoms]]></category>
		<category><![CDATA[women]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7171</guid>
		<description><![CDATA[Decreased sex drive in women is often a symptom age-related hormonal imbalances, but could also be side effects associated with certain medications.<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/decreased-sex-drive-in-women-a-symptom-or-side-effect.html">Decreased Libido in Women: A Symptom or Side Effect?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/decreased-sex-drive-in-women-a-symptom-or-side-effect.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>Cold Hands and Feet: Symptoms or Side Effects?</title>
		<link>http://www.usrecallnews.com/2009/10/cold-hands-and-feet-symptoms-or-side-effects.html</link>
		<comments>http://www.usrecallnews.com/2009/10/cold-hands-and-feet-symptoms-or-side-effects.html#comments</comments>
		<pubDate>Thu, 01 Oct 2009 01:20:53 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[cold feet]]></category>
		<category><![CDATA[cold hands]]></category>
		<category><![CDATA[digitek]]></category>
		<category><![CDATA[digoxin]]></category>
		<category><![CDATA[hypothyroidism]]></category>
		<category><![CDATA[metoprolol]]></category>
		<category><![CDATA[poor circulation]]></category>
		<category><![CDATA[side effects]]></category>
		<category><![CDATA[symptoms]]></category>
		<category><![CDATA[thyroid]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7149</guid>
		<description><![CDATA[Cold hands and feet are often symptoms of conditions or diseases such as low thyroid hormone, but could also be side effects associated with certain medications.<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/cold-hands-and-feet-symptoms-or-side-effects.html">Cold Hands and Feet: Symptoms or Side Effects?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/cold-hands-and-feet-symptoms-or-side-effects.html/feed</wfw:commentRss>
		<slash:comments>4</slash:comments>
		</item>
		<item>
		<title>Bone Fractures: Symptoms or Side Effects?</title>
		<link>http://www.usrecallnews.com/2009/10/bone-fractures-symptoms-or-side-effects.html</link>
		<comments>http://www.usrecallnews.com/2009/10/bone-fractures-symptoms-or-side-effects.html#comments</comments>
		<pubDate>Thu, 01 Oct 2009 01:16:52 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[avandia]]></category>
		<category><![CDATA[bone fractures]]></category>
		<category><![CDATA[conditions]]></category>
		<category><![CDATA[diseases]]></category>
		<category><![CDATA[fosamax]]></category>
		<category><![CDATA[osteoporosis]]></category>
		<category><![CDATA[side effects]]></category>
		<category><![CDATA[symtpoms]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7146</guid>
		<description><![CDATA[Bone fractures are often a symptom of conditions or diseases like osteoporosis, but could also be side effects associated with certain medications, such as these.<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/bone-fractures-symptoms-or-side-effects.html">Bone Fractures: Symptoms or Side Effects?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/bone-fractures-symptoms-or-side-effects.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Insomnia and Depression: Symptoms or Side Effects?</title>
		<link>http://www.usrecallnews.com/2009/10/insomnia-and-depression-symptoms-or-side-effects.html</link>
		<comments>http://www.usrecallnews.com/2009/10/insomnia-and-depression-symptoms-or-side-effects.html#comments</comments>
		<pubDate>Thu, 01 Oct 2009 01:09:03 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[chantix]]></category>
		<category><![CDATA[depression]]></category>
		<category><![CDATA[epilepsy]]></category>
		<category><![CDATA[insomnia]]></category>
		<category><![CDATA[Lexapro]]></category>
		<category><![CDATA[Pseudoephedrine]]></category>
		<category><![CDATA[ptsd]]></category>
		<category><![CDATA[Singulair]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7143</guid>
		<description><![CDATA[Insomnia and depression are often symptoms that show up in the same conditions like PTSD, but could also be side effects associated with certain medications.<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/insomnia-and-depression-symptoms-or-side-effects.html">Insomnia and Depression: Symptoms or Side Effects?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/10/insomnia-and-depression-symptoms-or-side-effects.html/feed</wfw:commentRss>
		<slash:comments>0</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>Shortness of Breath and Fatigue: Symptoms or Side Effects?</title>
		<link>http://www.usrecallnews.com/2009/09/shortness-of-breath-and-fatigue-symptoms-or-side-effects.html</link>
		<comments>http://www.usrecallnews.com/2009/09/shortness-of-breath-and-fatigue-symptoms-or-side-effects.html#comments</comments>
		<pubDate>Sat, 26 Sep 2009 20:42:09 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[fatigue]]></category>
		<category><![CDATA[shortness of breath]]></category>
		<category><![CDATA[side effects]]></category>
		<category><![CDATA[symptoms]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7121</guid>
		<description><![CDATA[Shortness of breath and fatigue are often symptoms of conditions like respiratory disease, but could also be side effects associated with certain medications.<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/shortness-of-breath-and-fatigue-symptoms-or-side-effects.html">Shortness of Breath and Fatigue: Symptoms or Side Effects?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/shortness-of-breath-and-fatigue-symptoms-or-side-effects.html/feed</wfw:commentRss>
		<slash:comments>1</slash:comments>
		</item>
		<item>
		<title>Skin Rashes: Symptoms or Side Effects?</title>
		<link>http://www.usrecallnews.com/2009/09/skin-rashes-symptoms-or-side-effects.html</link>
		<comments>http://www.usrecallnews.com/2009/09/skin-rashes-symptoms-or-side-effects.html#comments</comments>
		<pubDate>Sat, 26 Sep 2009 20:32:59 +0000</pubDate>
		<dc:creator>E. Sizemore</dc:creator>
				<category><![CDATA[Symptoms & Side Effects]]></category>
		<category><![CDATA[side effects]]></category>
		<category><![CDATA[skin rash]]></category>
		<category><![CDATA[skin rashes]]></category>
		<category><![CDATA[symptoms]]></category>

		<guid isPermaLink="false">http://www.usrecallnews.com/?p=7117</guid>
		<description><![CDATA[Skin rashes are often symptoms of conditions like allergies, eczema or poison ivy, but could also be side effects associated with certain medications.<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/skin-rashes-symptoms-or-side-effects.html">Skin Rashes: Symptoms or Side Effects?</a></p>
]]></description>
		<wfw:commentRss>http://www.usrecallnews.com/2009/09/skin-rashes-symptoms-or-side-effects.html/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
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