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	<title>Medical Product Guide&#187; Recalls</title>
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	<description>A comprehensive guide to medical products for medical professionals</description>
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		<title>Actavis US unit recalls Digitek tablets</title>
		<link>http://blog.medicalproductguide.com/2008/07/09/actavis-us-unit-recalls-digitek-tablets/</link>
		<comments>http://blog.medicalproductguide.com/2008/07/09/actavis-us-unit-recalls-digitek-tablets/#comments</comments>
		<pubDate>Wed, 09 Jul 2008 19:46:05 +0000</pubDate>
		<dc:creator>Jim Marino</dc:creator>
				<category><![CDATA[Cardiology products]]></category>
		<category><![CDATA[Pharmaceutical products]]></category>
		<category><![CDATA[Recalls]]></category>
		<category><![CDATA[Actavis]]></category>
		<category><![CDATA[Actavis Totowa]]></category>
		<category><![CDATA[digitalis toxicity]]></category>
		<category><![CDATA[Digitek]]></category>
		<category><![CDATA[digoxin]]></category>
		<category><![CDATA[heart failure]]></category>
		<category><![CDATA[renal failure]]></category>
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		<description><![CDATA[Actavis Group’s U.S. division, Actavis Totowa LLC, has recalled all lots of heart failure treatment Digitek (digoxin tablets). The company announced the Class I nationwide recall for Digitek after the possible commercial release of tablets with twice the approved level of the active ingredient, posing a risk of digitalis toxicity in patients with renal failure. [...]]]></description>
			<content:encoded><![CDATA[<p><img vspace="5" align="right" width="200" src="http://blog.medicalproductguide.com/files/2008/05/actavis.png" hspace="5" alt="Actavis" height="73" /><a href="http://www.actavis.com">Actavis Group</a>’s U.S. division, <a href="http://www.actavis.us/">Actavis Totowa LLC</a>, has recalled all lots of heart failure treatment Digitek (digoxin tablets). The company announced the Class I nationwide recall for Digitek after the possible commercial release of tablets with twice the approved level of the active ingredient, posing a risk of digitalis toxicity in patients with renal failure. Digitalis toxicity can cause nausea, vomiting, dizziness, low blood pressure, cardiac instability, bradycardia and death.</p>
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		<title>Herbal Science International recalls 12 dietary supplements</title>
		<link>http://blog.medicalproductguide.com/2008/04/16/herbal-science-international-recalls-12-dietary-supplements/</link>
		<comments>http://blog.medicalproductguide.com/2008/04/16/herbal-science-international-recalls-12-dietary-supplements/#comments</comments>
		<pubDate>Wed, 16 Apr 2008 11:08:11 +0000</pubDate>
		<dc:creator>Jim Marino</dc:creator>
				<category><![CDATA[Recalls]]></category>
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		<description><![CDATA[Herbal Science International Inc is recalling twelve dietary supplements that contain ephedra, aristolochic acid or human placenta because they may present a serious health hazard to consumers. FDA has long regarded dietary supplements containing ephedra as potential health hazards because this botanical contains ephedrine alkaloids. Recent studies have confirmed that ephedrine alkaloids raise blood pressure [...]]]></description>
			<content:encoded><![CDATA[<p>Herbal Science International Inc is recalling twelve dietary supplements that contain ephedra, aristolochic acid or human placenta because they may present a serious health hazard to consumers. FDA has long regarded dietary supplements containing ephedra as potential health hazards because this botanical contains ephedrine alkaloids. Recent studies have confirmed that ephedrine alkaloids raise blood pressure and cause stress to the circulatory system, effects that are linked to adverse health conditions such as heart attacks and strokes.</p>
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		<title>J&amp;J unit recalls 25 mcg/hr Duragesic patches</title>
		<link>http://blog.medicalproductguide.com/2008/02/18/jj-unit-recalls-25-mcghr-duragesic-patches/</link>
		<comments>http://blog.medicalproductguide.com/2008/02/18/jj-unit-recalls-25-mcghr-duragesic-patches/#comments</comments>
		<pubDate>Mon, 18 Feb 2008 18:08:05 +0000</pubDate>
		<dc:creator>Jim Marino</dc:creator>
				<category><![CDATA[Recalls]]></category>
		<category><![CDATA[Duragesic]]></category>
		<category><![CDATA[fentanyl]]></category>
		<category><![CDATA[Johnson & Johnson]]></category>
		<category><![CDATA[Pricara]]></category>
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		<description><![CDATA[Johnson &#38; Johnson&#8217;s PriCara unit has voluntarily recalled all lots of 25-microgram-per-hour Duragesic CII pain patches that have an expiration date of on or before December 2009. The recall is due to a possible cut in the lining of the internal reservoir that could cause the gel to leak. Direct exposure to the fentanyl drug [...]]]></description>
			<content:encoded><![CDATA[<p>Johnson &amp; Johnson&#8217;s PriCara unit has voluntarily recalled all lots of 25-microgram-per-hour Duragesic CII pain patches that have an expiration date of on or before December 2009. The recall is due to a possible cut in the lining of the internal reservoir that could cause the gel to leak. Direct exposure to the fentanyl drug can cause serious events, such as breathing problems, or even a potentially fatal overdose.</p>
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		<title>Chattem recalls its Icy Hot Heat Therapy products</title>
		<link>http://blog.medicalproductguide.com/2008/02/12/chattem-recalls-its-icy-hot-heat-therapy-products/</link>
		<comments>http://blog.medicalproductguide.com/2008/02/12/chattem-recalls-its-icy-hot-heat-therapy-products/#comments</comments>
		<pubDate>Tue, 12 Feb 2008 21:09:28 +0000</pubDate>
		<dc:creator>Jim Marino</dc:creator>
				<category><![CDATA[Recalls]]></category>
		<category><![CDATA[burns]]></category>
		<category><![CDATA[Chattem]]></category>
		<category><![CDATA[Icy Hot]]></category>
		<category><![CDATA[Icy Hot Heat Therapy]]></category>
		<category><![CDATA[product recall]]></category>
		<category><![CDATA[skin irritation]]></category>
		<guid isPermaLink="false">http://www.medicalproductguide.com/blog/2008/02/12/chattem-recalls-its-icy-hot-heat-therapy-products/</guid>
		<description><![CDATA[Chattem Inc. has voluntarily recalled its Icy Hot Heat Therapy products, following reports of skin irritation and first, second and third degree burns. The recalled products include Icy Hot Heat Therapy Air Activated Heat &#8211; Back, Icy Hot Heat Therapy Air Activated Heat &#8211; Arm, Neck, and Leg and Icy Hot Heat Therapy Air Activated [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.chattem.com/">Chattem Inc.</a> has voluntarily recalled its <a href="http://www.icyhot.com/">Icy Hot Heat Therapy</a> products, following reports of skin irritation and first, second and third degree burns. The recalled products include Icy Hot Heat Therapy Air Activated Heat &#8211; Back, Icy Hot Heat Therapy Air Activated Heat &#8211; Arm, Neck, and Leg and Icy Hot Heat Therapy Air Activated Heat &#8211; Arm, Neck, and Leg single consumer use (samples). Company spokesperson Catherine Baker said, “Because we are unsure if it is misuse or not, we’re going to study that before we make the decision to put the product back on the market or not.”</p>
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