<?xml version="1.0" encoding="UTF-8" ?>



	

<RECALLS_DATA>
<PRODUCT>
	<DATE>Mon, 20 May 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Sandoz]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Methotrexate Sodium, USP, 25 mg/mL, 40 mL vial injectable vials]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particulate material in vials]]></REASON>
	<COMPANY><![CDATA[Sandoz US]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm353291.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 15 May 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Pentec Health]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[In-date nutritional prescriptions for renal patients]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance]]></REASON>
	<COMPANY><![CDATA[Pentec Health]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm352861.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 10 May 2013 20:33:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Piperacillin and Tazobactam for Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Precipitation/Crystallization in IV bag]]></REASON>
	<COMPANY><![CDATA[Apotex Corp.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm351865.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 10 May 2013 15:25:00 -0400</DATE>
	<BRAND_NAME><![CDATA[SexVoltz, Velextra, Amerect]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplements used as a sexual enhancement product]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Products may contain undeclared tadalafil]]></REASON>
	<COMPANY><![CDATA[BeaMonstar Products]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm351847.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 07 May 2013 19:44:00 -0400</DATE>
	<BRAND_NAME><![CDATA[SexVoltz, Velextra, Amerect]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplements used as a sexual enhancement product]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Products may contain undeclared tadalafil]]></REASON>
	<COMPANY><![CDATA[BeaMonstar Products]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm351162.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 07 May 2013 12:51:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Lightning Rod]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contain an analogue of Sildenafil]]></REASON>
	<COMPANY><![CDATA[Chang Kwung Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm351058.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 06 May 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[The Compounding Shop LLC]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Compounded Products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Concerns associated with quality control procedures that present potential risk to sterility assurance]]></REASON>
	<COMPANY><![CDATA[The Compounding Shop LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm351841.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 01 May 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Vicerex, Black Ant]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared Active Ingredients]]></REASON>
	<COMPANY><![CDATA[American Lifestyle]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm350574.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 26 Apr 2013 13:52:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Piperacillin and Tazobactam for Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Precipitation/Crystallization in IV bag]]></REASON>
	<COMPANY><![CDATA[Apotex Corp.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm349976.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 26 Apr 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[0.9% Sodium Chloride Injection, USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particulates]]></REASON>
	<COMPANY><![CDATA[Hospira Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm349552.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 22 Apr 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Nora Apothecary &amp; Alternative Therapies]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[All Sterile Compounded Drug Products within Expiration]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of Sterility Assurance]]></REASON>
	<COMPANY><![CDATA[Nora Apothecary &amp; Alternative Therapies]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm349040.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 17 Apr 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Balanced Solutions Compounding Pharmacy]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sterile drug products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance.]]></REASON>
	<COMPANY><![CDATA[Balanced Solutions Compounding Pharmacy, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm348723.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 15 Apr 2013 22:36:00 -0400</DATE>
	<BRAND_NAME><![CDATA[NuVision Pharmacy]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Lyophilized compounds HcG 5000IU-5ml and Sermorelin/GHRH6-5ml]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance]]></REASON>
	<COMPANY><![CDATA[NuVision Pharmacy]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm348095.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 15 Apr 2013 22:18:00 -0400</DATE>
	<BRAND_NAME><![CDATA[ApothéCure]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sterile drug products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance]]></REASON>
	<COMPANY><![CDATA[ApothéCure Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm348094.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 10 Apr 2013 19:49:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Affirm XL]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contain an analogue of sildenafil]]></REASON>
	<COMPANY><![CDATA[Affirm XL]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm347558.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 05 Apr 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Green Valley Drugs]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sterile, compounded products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance and concerns associated with the quality control processes]]></REASON>
	<COMPANY><![CDATA[Green Valley Drugs]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm347559.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 01 Apr 2013 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[ROCK-IT-MAN]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Male sexual enhancement capsules]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Product contains hydroxythiohomosildenafil, an analogue of sildenafil]]></REASON>
	<COMPANY><![CDATA[Consumer Concepts, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm347026.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 29 Mar 2013 18:58:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sodium Chloride Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Brass particulates]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm345963.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 26 Mar 2013 22:08:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Pallimed Solutions, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sterile compounded drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Visible particulates]]></REASON>
	<COMPANY><![CDATA[Pallimed Solutions, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm345468.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 20 Mar 2013 19:53:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Med Prep Consulting, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[All compounded products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Due To Potential Mold Contamination]]></REASON>
	<COMPANY><![CDATA[Med Prep Consulting, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm344787.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 20 Mar 2013 19:28:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Clinical Specialties]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Acetylcysteine 10% solution, Cyclosporine 1% ophthalmic drops, Dexamethasone NaPo4 12 mg/ml, more]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance]]></REASON>
	<COMPANY><![CDATA[Clinical Specialties Compounding Pharmacy]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm344786.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 18 Mar 2013 19:09:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Avastin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Avastin unit dose syringes]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[The product has or potentially could result in an infection within the eye]]></REASON>
	<COMPANY><![CDATA[Clinical Specialties]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm344377.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sun, 17 Mar 2013 19:38:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Med Prep Consulting, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[All compounded products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[DUE TO POTENTIAL MOLD CONTAMINATION]]></REASON>
	<COMPANY><![CDATA[Med Prep Consulting, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm344229.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 16 Mar 2013 20:25:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Med Prep Consulting, Inc]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[MAGNESIUM SULFATE 2GM IN DEXTROSE 5 PERCENT IN WATER, 50 ml FOR INJECTION]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contain visible particulate contaminants confirmed to be mold]]></REASON>
	<COMPANY><![CDATA[Med Prep Consulting, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm344189.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 11 Mar 2013 15:24:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Night Bullet]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Product contains trace amounts of Sulfohydroxyhomosildenafil and Aminotadalafil.]]></REASON>
	<COMPANY><![CDATA[Green Planet, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm343216.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 23 Feb 2013 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[OMONTYS&amp;reg;]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[OMONTYS&amp;reg; (peginesatide) Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Serious hypersensitivity reactions, including anaphylaxis]]></REASON>
	<COMPANY><![CDATA[Affymax, Inc. and Takeda Pharmaceutical Company Limited]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm340893.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 21 Feb 2013 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Maxiloss Weight Advanced]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Olaax Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm340921.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 15 Feb 2013 20:35:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Vistide]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[cidofovir injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particulate matter]]></REASON>
	<COMPANY><![CDATA[Gilead Sciences Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm340091.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 15 Feb 2013 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Reumofan Plus]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Tablets contain undeclared active pharmaceutical ingredients: methocarbamol, dexamethasone, and diclofenac]]></REASON>
	<COMPANY><![CDATA[Reumofan Plus USA, LLC  and Reumofan USA, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm340161.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 25 Jan 2013 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Lactated Ringers and 5% Dextrose Injection, USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain spore like particulate]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm336959.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 24 Jan 2013 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Super Power]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[D&amp;amp;S Herbals, LLC, d/b/a Freedom Trading]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm337019.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 17 Jan 2013 19:55:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Rugby]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Ferrous Sulfate Tablets, 325 mg]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Bottle of Ferrous Sulfate Tablets, 325 mg, may actually contain Meclizine HCl 25 mg tablets]]></REASON>
	<COMPANY><![CDATA[Advance Pharmaceutical Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm336107.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 10 Jan 2013 11:02:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Mitosol]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Mitomycin for solution]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May be non-sterile]]></REASON>
	<COMPANY><![CDATA[MobiusTherapeutics, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm335055.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 21 Dec 2012 10:15:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Slimdia Revolution]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contain Sibutramine, an active drug ingredient not listed on label]]></REASON>
	<COMPANY><![CDATA[P&amp;J TRADING]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm333178.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 20 Dec 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[UDL Laboratories, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[tablets may exceed the weight requirement and could exceed the label claim potency requirements for the ingredients hydrocodone bitartrate and acetaminophen]]></REASON>
	<COMPANY><![CDATA[Mylan Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm333153.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 18 Dec 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Zicam]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Nasal Spray]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Burkholderia cepacia]]></REASON>
	<COMPANY><![CDATA[Matrixx Initiatives]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm332787.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 17 Dec 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Libigrow XXXtreme, Blue Diamond, Blue Diamond Platinum, Mojo Nights, Mojo Nights Supreme, and Casanova]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Performance Plus Marketing, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm332697.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 14 Dec 2012 21:04:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Carboplatin Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Presence of visible particulates.]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm332353.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 06 Dec 2012 22:39:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Qualitest]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hydrocodone bitartrate and acetaminophen 10mg/500 mg tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Tablets from the affected lots may exceed the weight requirement and could exceed the label claim potency requirements for the ingredients of hydrocodone bitartrate and acetaminophen.]]></REASON>
	<COMPANY><![CDATA[Qualitest]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm331218.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 29 Nov 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[GlideScope]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[GVL Video Laryngoscopes reusable blades]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Laryngoscope blades have been found to be prone to developing cracks and/or breaking across the tip of the blade, which potentially could result in pieces of the blade breaking off in patient’s mouths and obstructing the airway or being swallowed]]></REASON>
	<COMPANY><![CDATA[Verathon Inc]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm330305.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 28 Nov 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Atorvastatin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Atorvastatin Calcium Tablets (10 mg, 20 mg and 40 mg)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain very small glass particles resembling a fine grain of sand (less than 1 mm in size)]]></REASON>
	<COMPANY><![CDATA[Ranbaxy Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm329866.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 27 Nov 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Isovue]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Pre-Filled Power Injector Syringes]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Presence of visible particulate matter in syringes]]></REASON>
	<COMPANY><![CDATA[Bracco Diagnostics Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm329740.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 31 Oct 2012 14:08:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Ameridose]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Sterility]]></REASON>
	<COMPANY><![CDATA[Ameridose, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm326349.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 24 Oct 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Classic Zi Xiu Tang Bee Pollen and Ultimate Formula]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared Sibutramine]]></REASON>
	<COMPANY><![CDATA[Zi Xiu Tang Success, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm326267.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 19 Oct 2012 17:09:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Banana Boat and Ultra Defense]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Continuous spray sun care products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Potential risk of product igniting on the skin if contact is made with a source of ignition before the product is completely dry]]></REASON>
	<COMPANY><![CDATA[Energizer Holdings Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm324824.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 06 Oct 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[NECC]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Methylprednisolone Acetate, Betamethasone, Bupivicaine, more]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Sterility; linkage to meningitis outbreak]]></REASON>
	<COMPANY><![CDATA[New England Compounding Center (NECC)]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm322901.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 05 Oct 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Lactated Ringer’s and 5% Dextrose]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Container Leak and mold contamination]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm322961.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 20 Sep 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Watson]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hydrocodone Bitartrate and APAP Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Tablets are thicker and darker than specification]]></REASON>
	<COMPANY><![CDATA[Watson Laboratories, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm320566.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 12 Sep 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[ACTRA-Sx 500]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Body Basics, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm319697.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 10 Sep 2012 16:02:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Qualitest]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hydrocodone Bitartrate &amp; Acetaminophen Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Tablets may exceed weight specification and could be super-potent for the ingredients Hydrocodon Bitartrate &amp; Acetaminophen]]></REASON>
	<COMPANY><![CDATA[Qualitest]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm318827.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 04 Sep 2012 13:45:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Sun Pharmaceutical Industries]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Nimodipine Capsules, 30 mg]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain crystals of nimodipine]]></REASON>
	<COMPANY><![CDATA[Sun Pharmaceutical Industries, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm318118.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 24 Aug 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Samantha Lynn Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Reumofan Plus Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredients, methocarbamol, dexamethasone  and diclofenac]]></REASON>
	<COMPANY><![CDATA[Samantha Lynn Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm317248.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 23 Aug 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Mojo Nights]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved New Drug]]></REASON>
	<COMPANY><![CDATA[Evol Nutrition Associates, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm320397.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 15 Aug 2012 21:07:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hydromorphone Injection, USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain more than the 1 mL labeled fill volume]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm315671.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 14 Aug 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Propofol Injectable Emulsion]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Visible particles embedded in the glass]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm315719.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 25 Jul 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[DUKAL, Zee]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Benzalkonium chloride swabs and antiseptic wipes]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[potential microbial contamination with Burkholderia cepacia]]></REASON>
	<COMPANY><![CDATA[DUKAL Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm313912.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 20 Jul 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[X-ROCK 3 Day Pill and Z-ROCK]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[X-ROCK 3 Day Pill and Z-ROCK]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared sildenafil]]></REASON>
	<COMPANY><![CDATA[CRM Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm313141.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 13 Jul 2012 18:13:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Injectable carboplatin, cytarabine, paclitaxel, and methotrexate]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[visible particles embedded in the glass located at the neck of the vial]]></REASON>
	<COMPANY><![CDATA[Hospira Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm311971.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 03 Jul 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Bedford Laboratories]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Leucovorin Calcium Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Crystalline particulate matter]]></REASON>
	<COMPANY><![CDATA[Bedford Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm310666.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 28 Jun 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Bedford Laboratories]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Vecuronium Bromide Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particulate matter]]></REASON>
	<COMPANY><![CDATA[Bedford Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm310191.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 05 Jun 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Introvale]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Oral Contraceptive]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Packaging flaw]]></REASON>
	<COMPANY><![CDATA[Sandoz Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm307098.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 26 May 2012 16:21:00 -0400</DATE>
	<BRAND_NAME><![CDATA[V Maxx]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[V Maxx Rx]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared sulfoaidenafil]]></REASON>
	<COMPANY><![CDATA[The Menz Club, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm305795.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 25 May 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Franck&quot;s]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sterile Human and Veterinary Prescription Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Presence of microorganisms and fungal growth]]></REASON>
	<COMPANY><![CDATA[Franck&#39;s Compounding Lab]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm305509.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 18 May 2012 22:15:00 -0400</DATE>
	<BRAND_NAME><![CDATA[FIRMINITE, EXTRA STRENGTH INSTANT HOT ROD, AND LIBIDRON]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drug for Erectile Dysfunction (ED)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[West Coast Nutritionals, Ltd.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm304719.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 12 May 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hydromorphone Injection, USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain more than the 1 mL labeled fill volume]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm303942.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 02 May 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Franck&#39;s]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Triamcinolone acetonide P.F. 80mg/ml]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Possible fungal contamination]]></REASON>
	<COMPANY><![CDATA[Franck&#39;s Compounding Lab]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm302899.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 24 Apr 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Epinephrine Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Discoloration and Small Visible Particles]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm301783.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 19 Apr 2012 16:42:00 -0400</DATE>
	<BRAND_NAME><![CDATA[X-ROCK]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Product Marketed as a Dietary Supplement To Support Male Sexual Performance]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Product contains sildenafil and hydroxythiohomosildenafil]]></REASON>
	<COMPANY><![CDATA[XROCK INDUSTRIES]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm301210.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 17 Apr 2012 16:56:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Morphine Sulfate Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Carpujects syringes contain more than the 1 mL labeled fill volume]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm300813.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 02 Apr 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Cyanocobalamin Injection, USP, (1000 mcg/mL), 1mL Vial]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[crack can form on the bottom and sides of vials]]></REASON>
	<COMPANY><![CDATA[Luitpold Pharmaceuticals Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm298545.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 31 Mar 2012 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Frank&#39;s]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Triamcinolone acetonide P.F. 80mg/ml]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Possible fungal contamination]]></REASON>
	<COMPANY><![CDATA[Franck&#39;s Compounding Lab]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm300712.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 09 Mar 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Franck&#39;s]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Brilliant Blue G]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Possible fungal contamination]]></REASON>
	<COMPANY><![CDATA[Franck&#39;s Compounding Lab]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm296326.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 24 Feb 2012 18:04:00 -0500</DATE>
	<BRAND_NAME><![CDATA[RegenErect]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Intimacy Enhancement Capsule]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Regeneca, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm293376.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 24 Feb 2012 16:17:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Glenmark Generics, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Norgestimate and Ethinyl Estradiol Tablets USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Packaging error potentially causing incorrect dosing regimen]]></REASON>
	<COMPANY><![CDATA[Glenmark Generics, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm293347.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 22 Feb 2012 17:47:00 -0500</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Phenylephrine HCl Injection USP 1%]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Visible particles were found in the product]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm292951.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 22 Feb 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Healthy People Co.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredients]]></REASON>
	<COMPANY><![CDATA[Healthy People Co.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm292796.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 17 Feb 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[TYLENOL]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Infants TYLENOL Oral Suspension, 1 oz. Grape]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[difficulty using the Infants TYLENOL SimpleMeasure dosing system]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm292537.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 16 Feb 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Bedford Laboratories]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Cytarabine for Injection USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Lack of sterility assurance]]></REASON>
	<COMPANY><![CDATA[Bedford Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm293076.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 10 Feb 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[RegenArouse]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Intimacy Enhancement Capsule]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Regeneca, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm291546.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 09 Feb 2012 21:05:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Koff &amp; Kold, Kold Sore]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[OTC drug products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Non-sterile, intended for use in eyes and nose.]]></REASON>
	<COMPANY><![CDATA[Wholistic Herbs, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm291386.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 06 Feb 2012 16:05:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Crickit]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Surgical Crichothyroidotomy Kit]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Kit contains recalled povidone iodine prep pads]]></REASON>
	<COMPANY><![CDATA[North American Rescue, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm290639.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 02 Feb 2012 16:43:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Bedford Laboratories]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Acetylcysteine Solution, USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Visible glass particle found in a vial.]]></REASON>
	<COMPANY><![CDATA[Bedford Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm290204.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 31 Jan 2012 19:33:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Lo/Ovral-28]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Oral contraceptives]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Some blister packs may contain an inexact count of inert or active ingredient tablets and the tablets may be out of sequence.]]></REASON>
	<COMPANY><![CDATA[Pfizer, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm289770.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 27 Jan 2012 18:05:00 -0500</DATE>
	<BRAND_NAME><![CDATA[AVEENO&amp;reg; BABY CALMING COMFORT&amp;reg;]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Lotion]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[The lot exceeded bacterial specifications.]]></REASON>
	<COMPANY><![CDATA[Johnson &amp; Johnson Consumer Companies, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm289619.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 27 Jan 2012 14:48:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Cephalon]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Treanda (bendamustine HCL) for Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Presence of particulate matter in vial identified as glass fragments]]></REASON>
	<COMPANY><![CDATA[Cephalon]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm289452.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 19 Jan 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Perfect Image Solutions]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hair regrowth products (men &amp; women)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[The products are deemed unapproved new drugs under the law and U.S. Food and Drug Administration regulations and may present potential health hazards]]></REASON>
	<COMPANY><![CDATA[Perfect Image Solutions LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm288505.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 18 Jan 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Female One Series]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Vagifresh Ball, Vagifresh Gel]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Vagifresh Gel sample contains benzocaine, the active ingredient for many anesthetic drug products. 
Vagifresh Ball sample contains bacteria including Staphylococcus lentus, S. sciuri, Bacillus lantus, Alloiococcus otitis, Aerococcus viridans, Aeromonas salmonicid, Gemella spp, Leuconostoc spp.]]></REASON>
	<COMPANY><![CDATA[USA Far Ocean Group (U.S.A. Far Ocean)]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm288260.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 10 Jan 2012 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Bedford Laboratories]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Polymyxin B for Injection USP and Vecuronium Bromide]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Vials may contain visible glass particulates]]></REASON>
	<COMPANY><![CDATA[Bedford Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm286953.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sun, 08 Jan 2012 20:16:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Excedrin, NoDoz, Bufferin, Gas-X]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Bufferin Extra Strength Tablet, Bufferin Low Dose Tablets, Bufferin Regular Strength Tablets, Excedrin Back &amp; Body Caplets, Excedrin Extra Strength Caplets, Excedrin Extra Strength  Express Gel Caps, Excedrin Extra Strength  Gel Tablets, Excedrin Extra Strength  Tablets, Excedrin Migraine  Express Gel Caplets, Excedrin Migraine Caplets,  Excedrin Migraine Gel Tablets, Excedrin Migraine Tablets, Excedrin PM Caplets, Excedrin PM Express Gel Caplet, Excedrin PM Tablets, Excedrin Sinus Headache Caplets, Excedrin Tension Headache Caplets, Excedrin Tension Headache Express Gel Caplets, Excedrin Tension Headache Gel Tablets, Gas-X Prevention Caplets, NoDoz Maximum Strength Caplets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[products may contain stray tablets, capsules, or caplets from other Novartis products, or contain broken or chipped tablets]]></REASON>
	<COMPANY><![CDATA[Novartis]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm286240.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 21 Dec 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Motrin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Motrin IB Coated Tablets and Motrin IB Coated Caplets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May not dissolve as quickly as intended]]></REASON>
	<COMPANY><![CDATA[McNeil]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm284942.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 02 Dec 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Argatroban]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Argatroban Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Potential for presence of visible particulates]]></REASON>
	<COMPANY><![CDATA[Eagle Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm297069.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 10 Nov 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Virility Max]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Virility Max Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains undeclared drug ingredient sulfoaildenafil]]></REASON>
	<COMPANY><![CDATA[Keime, Incorporated]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm279659.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 19 Oct 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Nostrilla]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Nasal Decongestant]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain the bacteria Burkholderia cepacia]]></REASON>
	<COMPANY><![CDATA[Insight Pharmaceuticals, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm276721.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 03 Oct 2011 10:42:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Uprizing 2.0]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Testosterone Booster]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared Superdrol]]></REASON>
	<COMPANY><![CDATA[Superior Metabolic Technologies, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm274507.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 15 Sep 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Cyclafem, Emoquette, Gildess, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Oral contraceptives]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Packaging error]]></REASON>
	<COMPANY><![CDATA[Qualitest Pharmaceuticals]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm272199.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 02 Sep 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Slim Forte, Meizitang Botanical]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Slimming capsules and coffee]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared Sibutramine]]></REASON>
	<COMPANY><![CDATA[Intercharm Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm265705.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 24 Aug 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[H&amp;P Industries]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Povidone Iodine products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Processed without following drug manufacturing requirements]]></REASON>
	<COMPANY><![CDATA[H&amp;P Industries, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm269642.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 02 Aug 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Vasopressin Injection USP, multiple strengths and sizes]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Sub-potency]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm266615.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 18 Jul 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Calcium Gluconate Injection, USP, 10%, 100 mL Pharmacy Bulk Package]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Some vials may contain silicone particles]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm263531.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 13 Jul 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Via Xtreme]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Via Xtreme Ultimate Sexual Enhancer Dietary Supplement For Men]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains undeclared drug ingredients]]></REASON>
	<COMPANY><![CDATA[Global Wellness LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm263025.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 28 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[McNeil Consumer Healthcare]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[TYLENOL, Extra Strength Caplets, 225 count]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Uncharacteristic odor linked to trace amounts of 2,4,6 tribromoanisole]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm261498.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 24 Jun 2011 18:44:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Endocet]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Endocet (oxycodone/acetaminophen, USP) Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Some bottles contain different strength tablets]]></REASON>
	<COMPANY><![CDATA[Endo Pharmaceuticals]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm260826.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 24 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Qualitest]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Butalbital, Acetaminophen, and Caffeine Tablets USP; Hydrocodone Bitartrate and Acetaminophen  Tablets, USP]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Recalled bottles may contain incorrect tablets]]></REASON>
	<COMPANY><![CDATA[Qualitest Pharmaceuticals]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm260837.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 22 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Nature Relief]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Instant Wart and Mole Remover]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Can cause burns]]></REASON>
	<COMPANY><![CDATA[Nature Relief]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm260817.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 17 Jun 2011 17:43:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Ortho-McNeil-Janssen Pharmaceuticals, Inc.  and Patriot Pharmaceuticals, LLC]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[RISPERDAL, 3mg tablets and risperidone, 2mg tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Uncharacteristic odor thought to be caused by trace amounts of 2,4,6 tribromoanisole]]></REASON>
	<COMPANY><![CDATA[Ortho-McNeil-Janssen Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm259820.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 15 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Concentrated Sodium Chloride Injection, USP, 23.4%, 30 mL Single Dose Vial]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Some vials contain visible particulates]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm259312.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 13 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Bedford Laboratories]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Indomethacin for Injection, USP, 1mg Single Dose Vial]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Some of the vials may contain particulate matter]]></REASON>
	<COMPANY><![CDATA[Bedford Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm259237.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 06 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Via Xtreme]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredients]]></REASON>
	<COMPANY><![CDATA[Global Wellness LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm258055.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 06 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Methyldopate HCl Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Some of the vials contain translucent visible particles consistent with glass delamination]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm258064.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 01 Jun 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Aidapak Services]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[abacavir tablets, acarbose tablets, more]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[penicillin contamination]]></REASON>
	<COMPANY><![CDATA[Aidapak Services, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm257704.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 24 May 2011 15:59:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Slim Xtreme Herbal Slimming Capsule]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared Drug Ingredient]]></REASON>
	<COMPANY><![CDATA[Globe All Wellness, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm256649.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 19 May 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sterile Water for Injection, USP, 50 mL Single Dose Vial]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulate matter]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm256061.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 05 May 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Caffeine &amp; Sodium Benzoate Injection, USP, 250 mg/mL, 2 mL Single Dose Vial]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulates prior to expiration date]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm254287.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 02 May 2011 15:53:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Bristol-Myers Squibb]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Coumadin Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain higher than labeled amount of coumadin]]></REASON>
	<COMPANY><![CDATA[Bristol-Myers Squibb]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm253523.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 28 Apr 2011 23:34:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Regenerect]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Regenerect Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains undeclared drug ingredient sulfoaildenafil]]></REASON>
	<COMPANY><![CDATA[Ethos Environmental, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm253123.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 26 Apr 2011 17:32:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Ammonium Molybdate Injection, USP (Molybdenum 250mcg/10mL) 10mL Single Dose Vial]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulates prior to expiration date]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm252819.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 14 Apr 2011 13:05:00 -0400</DATE>
	<BRAND_NAME><![CDATA[TOPAMAX®]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[TOPAMAX® (topiramate) 100mg Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Uncharacteristic Odor]]></REASON>
	<COMPANY><![CDATA[Ortho-McNeil Neurologics Division]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm251515.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 29 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Meds IV]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Total Parenteral Nutrition Solutions and Others (See List Below)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Serratia marcescens]]></REASON>
	<COMPANY><![CDATA[Meds IV]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm249068.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 28 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[THE BEST]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[THE BEST Enhancement Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient, Sulfoaildenafil]]></REASON>
	<COMPANY><![CDATA[AVNS, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm249126.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 26 Mar 2011 16:53:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Greenstone]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Citalopram 10mg Tablets (100-count bottle) and Finasteride 5mg Tablets (90-count bottle)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Bottles may contain wrong drug]]></REASON>
	<COMPANY><![CDATA[Greenstone LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm248552.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 25 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[X-Hero, Male Enhancer]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[X-Hero and Male Enhancer Dietary Supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredients, Sulfosildenafil and Tadalafil]]></REASON>
	<COMPANY><![CDATA[USA Far Ocean Group, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm248718.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 25 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[APP Pharmaceuticals]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Irinotecan Hydrochloride Injection]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Fungal microbial contaminant particulate matter]]></REASON>
	<COMPANY><![CDATA[APP Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm248576.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 22 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[U-Prosta]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[U-Prosta Natural support for prostate health]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[product contains terazosin, the active ingredient of an FDA-approved drug used to treat Benign Prostatic Hyperplasia (enlarged prostate), making U-Prosta an unapproved drug]]></REASON>
	<COMPANY><![CDATA[USA Far Ocean Group Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm248116.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 16 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL, 1 mL Single Dose Vials; 5 mL and 30 mL Multiple Dose Vials]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulates prior to expiration date]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm247526.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 15 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Celerite]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement Tea]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient, Sibutramine]]></REASON>
	<COMPANY><![CDATA[Shaping Beauty, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm248388.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 15 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Cardinal Health, Triad, Total Resources, Others]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Povidone Iodine Prep Pads]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Elizabethkingia meningoseptica]]></REASON>
	<COMPANY><![CDATA[H&amp;P Industries, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm247658.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 15 Mar 2011 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Bacteriostatic Sodium Chloride Injection, USP, 0.9%, 30 mL Multiple Dose Vials]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain visible particulates]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm247402.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 05 Mar 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Smith and Nephew]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[IV PREP Antiseptic Wipes]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Potential contamination with Bacillus cereus]]></REASON>
	<COMPANY><![CDATA[Smith &amp; Nephew, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm246058.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 24 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Soothe® Xtra Protection (XP)]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Eye drops]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Out of specification for preservative efficacy]]></REASON>
	<COMPANY><![CDATA[Bausch + Lomb]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm277191.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 22 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[EXTENZE]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[EXTENZE nutritional supplement tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drugs: Sibutramine, Tadalafil, and Sildenafil]]></REASON>
	<COMPANY><![CDATA[Biotab Nutraceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm244329.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 18 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Amantadine, Amlodipine, Baclofen, Others]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Various drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Mislabeled bottles]]></REASON>
	<COMPANY><![CDATA[Upsher-Smith Laboratories, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm244111.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 16 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Jantoven]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Warfarin Sodium, USP, 3mg Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Mislabeled Bottles: 10mg strength tablets found in bottle labeled for 3mg tablets]]></REASON>
	<COMPANY><![CDATA[Upsher-Smith Laboratories, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm243811.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 09 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Svelte 30]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Svelte 30 Herb Supplement, orange &amp; gray capsules]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient: Sibutramine]]></REASON>
	<COMPANY><![CDATA[Svelte 30 Nutritional Consultants]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm244393.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 05 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[a) Hydrocodone Bitartrate and Acetaminophen Tablets

b)Phenobarbital Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Bottle may be incorrectly labeled]]></REASON>
	<COMPANY><![CDATA[Qualitest Pharmaceuticals]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm242398.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 04 Feb 2011 17:06:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Trelstar]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Watson’s Trelstar (triptorelin pamoate for injectable suspension) product, containing alcohol prep pads]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contain alcohol prep pads that were recently recalled by the Triad Group due to potential contamination with Bacillus cereus]]></REASON>
	<COMPANY><![CDATA[Watson Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm242359.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 03 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Potassium Phosphates Injection, USP, 15 mM/5 mL Phosphorus; 22 mEq/5 mL Potassium]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particles consistent with glass delamination]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm242331.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 03 Feb 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sodium Thiosulfate Injection, USP, 10%]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particles consistent with glass delamination]]></REASON>
	<COMPANY><![CDATA[American Regent, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm242195.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 31 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Fruta Planta]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Fruta Planta weight loss dietary supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Sibutramine, an undeclared drug ingredient]]></REASON>
	<COMPANY><![CDATA[Godi International, Corp.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm241835.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 26 Jan 2011 07:21:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Relistor]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Relistor kit containing alcohol prep pads]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains potentially contaminated alcohol prep pads]]></REASON>
	<COMPANY><![CDATA[Pfizer Inc. and Progenics  Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm241070.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 24 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Celerite]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Celerite Slimming Capsules]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Sibutramine, an undeclared drug ingredient]]></REASON>
	<COMPANY><![CDATA[Shaping Beauty, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm242199.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 24 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[GlaxoSmithKline]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[ARIXTRA Starter Kit containing alcohol prep pads]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains potentially contaminated alcohol prep pads]]></REASON>
	<COMPANY><![CDATA[GlaxoSmithKline]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm241097.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 20 Jan 2011 16:24:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Betaseron]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Betaseron kit containing alcohol prep pads]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains potentially contaminated alcohol prep pads]]></REASON>
	<COMPANY><![CDATA[Bayer HealthCare Pharmaceuticals]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm240558.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 18 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Stud, Nite Rider]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Nite Rider Maximum Sexual Enhancer For Men and STUD  Capsules for Men Male Enhancement Herbal Supplement Capsules Marketed as Dietary Supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Adulterated with Sildenafil, an FDA approved drug used in the treatment of Erectile Dysfunction (ED), making the products unapproved new drugs]]></REASON>
	<COMPANY><![CDATA[Kanec USA]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm240840.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 14 Jan 2011 19:13:00 -0500</DATE>
	<BRAND_NAME><![CDATA[TYLENOL, BENADRYL, SUDAFED PE]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[TYLENOL® 8 Hour, TYLENOL® Arthritis Pain, and TYLENOL® upper respiratory products, and certain lots of BENADRYL®, SUDAFED PE®, and SINUTAB®]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Production records found instances where equipment cleaning procedures were insufficient or that cleaning was not adequately documented.]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm240218.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 13 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Boniva, Fuseon, Pegasys, Others]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Medicine Kits]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Kits contain alcohol prep pads that were recently recalled by the Triad Group due to potential contamination with Bacillus cereus]]></REASON>
	<COMPANY><![CDATA[Genentech, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm240131.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 10 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Extavia]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Extavia kit containing alcohol prep pads]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contain alcohol prep pads that were recently recalled by the Triad Group due to potential contamination with Bacillus cereus]]></REASON>
	<COMPANY><![CDATA[Novartis Pharmaceuticals Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm241610.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 06 Jan 2011 12:27:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Teva Pharmaceuticals]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Metronidazole Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Underweight Tablets]]></REASON>
	<COMPANY><![CDATA[Teva Pharmaceuticals, U.S.A]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm239229.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 05 Jan 2011 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[VersaPro, Cardinal Health, PSS Select, Others]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Bacillus cereus]]></REASON>
	<COMPANY><![CDATA[Triad Group]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ucm239219.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 30 Dec 2010 16:38:00 -0500</DATE>
	<BRAND_NAME><![CDATA[RockHard Extreme, Passion Coffee]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Rock Hard Extreme and Passion Coffee Dietary Supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved drugs - contain an analog of Sildenafil]]></REASON>
	<COMPANY><![CDATA[Drive Total Energy]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm238492.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 30 Dec 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Albuterol Inhalation Solution]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect concentration listed]]></REASON>
	<COMPANY><![CDATA[The Ritedose Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm238528.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 23 Dec 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Sodium Bicarbonate Injection, USP, 7.5% 
and 8.4%, 50 mL Single Dose Vials]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulates]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm238227.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 22 Dec 2010 17:52:00 -0500</DATE>
	<BRAND_NAME><![CDATA[RockHard Weekend, Pandora]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[RockHard Weekend and Pandora dietary supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved drug - contain an analog of Sildenafil]]></REASON>
	<COMPANY><![CDATA[RockHard Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm237999.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 22 Dec 2010 14:17:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Lipitor]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Lipitor]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[off odor]]></REASON>
	<COMPANY><![CDATA[Pfizer]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm237938.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 20 Dec 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dexamethasone Sodium Phosphate Injection, USP, 4 mg/mL]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulates]]></REASON>
	<COMPANY><![CDATA[American Reagent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm238001.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 09 Dec 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Rolaids]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Rolaids Soft Chews]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Foreign materials, including metal and wood particles]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm236715.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 09 Dec 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Refenesen, Select, QC Medifin, Others]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Cold Decongestant Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Mislabeled: Acetaminophen, phenylephrine, and chlorpheniramine maleate not included]]></REASON>
	<COMPANY><![CDATA[Reese Pharmaceutical Company]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm236509.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 02 Dec 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Duro Extend]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplements, Duro Extend Capsules For Men]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved drug - contains  Sulfoaidenafil]]></REASON>
	<COMPANY><![CDATA[Intelli Health Products]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm235848.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 29 Nov 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Mylanta, Alternagel]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Mylanta and Alternagel Liquid Products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared alcohol from flavoring agents]]></REASON>
	<COMPANY><![CDATA[Johnson &amp; Johnson-Merck Consumer Pharmaceuticals, Co.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm235376.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 24 Nov 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Tylenol]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Tylenol Cold Liquid Products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Labeling update]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm234997.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 15 Nov 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Rolaids]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Uncharacteristic consistency or texture]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm234996.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 15 Nov 2010 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Benadryl, Motrin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Children&#39;s Benadryl, Children&#39;s Motrin]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Insufficiencies in the development of the manufacturing process]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm235002.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 27 Oct 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[B. Braun]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[heparin]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[trace amounts of contaminant]]></REASON>
	<COMPANY><![CDATA[B. Braun Medical Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm231639.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Sat, 23 Oct 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hyland]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Teething tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[The product may contain inconsistent amounts of the substance belladonna]]></REASON>
	<COMPANY><![CDATA[Standard Homeopathic Company]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm230769.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 21 Oct 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Actavis]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Fentanyl patch]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[released its active ingredient faster than the approved specification]]></REASON>
	<COMPANY><![CDATA[Actavis Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm230498.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 07 Oct 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Novedex XT]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Novedex XT]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain an Aromatase Inhibitor]]></REASON>
	<COMPANY><![CDATA[Gaspari Nutrition]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm228749.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 24 Sep 2010 14:54:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Epogen]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[EPOGEN® and PROCRIT® (Epoetin alfa) vials]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Glass flakes in vials]]></REASON>
	<COMPANY><![CDATA[Amgen]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm227202.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 16 Sep 2010 17:24:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Advanced Muscle Science]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Arom-X, Arom-X UTT, Arom-XL, 4-AD, and Decavol]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain an Aromatase Inhibitor]]></REASON>
	<COMPANY><![CDATA[Advanced Muscle Science]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm226145.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 16 Sep 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[IForce]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Reversitol capsules]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain an Aromatase Inhibitor]]></REASON>
	<COMPANY><![CDATA[Tribravus Enterprises, LLC d/b/a/ iForce Nutrition, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm226259.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 15 Sep 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Fizogen Precision Technologies]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Off Cycle II Hardcore]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain an Aromatase Inhibitor]]></REASON>
	<COMPANY><![CDATA[Fizogen Precision Technologies]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm226109.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 14 Sep 2010 20:06:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Clomed]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Clomed]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain an Aromatase Inhibitor]]></REASON>
	<COMPANY><![CDATA[KiloSports Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm225847.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 13 Sep 2010 21:53:00 -0400</DATE>
	<BRAND_NAME><![CDATA[G.E.T Genetic Edge Technologies, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[ArimaDex]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain an Aromatase Inhibitor]]></REASON>
	<COMPANY><![CDATA[Genetic Edge Technologies]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm225848.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 24 Aug 2010 16:47:00 -0400</DATE>
	<BRAND_NAME><![CDATA[MasXtreme]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplement capsules]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug substance: Aminotadalafil, an analog of tadalafil]]></REASON>
	<COMPANY><![CDATA[Natural Wellness, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm223937.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 18 Aug 2010 15:39:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Don Wands]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplement, Mr. Magic Male Enhancer]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug substance: Sulfoaildenafil and Hydroxythiosildenofil, analogues of Sildenafil]]></REASON>
	<COMPANY><![CDATA[Glow Industries, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm223082.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 18 Aug 2010 00:22:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Slim-30]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Slim-30 Herb Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug substance: Desmethyl Sibutramine]]></REASON>
	<COMPANY><![CDATA[J &amp; H Besta Corp.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm223141.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 10 Aug 2010 19:40:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Novacare]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement: Stiff Nights, Aziffa, Size Matters, Erex, Mojo, Hard Drive, Eyeful, Red Magic, Straight Up, Zotrex, Monster Excyte, WOW, Xaitrex, Verect, Prolatis, Xytamax, Maxyte, Libidinal, OMG, OMG45, Zilex (with Golden Spear)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug substance: Sulfoaildenafil]]></REASON>
	<COMPANY><![CDATA[Novacare, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm221958.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 09 Aug 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Prolatis’]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug substance: Sulfoaildenafil, an analogue of Sildenafil]]></REASON>
	<COMPANY><![CDATA[Prolatis’]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm222315.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 28 Jul 2010 17:56:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Ejaculoid XXTREME, Stimuloid II]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains undeclared drug ingredient]]></REASON>
	<COMPANY><![CDATA[Nutraloid Labs, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm220601.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 16 Jul 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Slim-30 Herb Supplement]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains undeclared drug ingredient]]></REASON>
	<COMPANY><![CDATA[J &amp; H Besta Corp.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm219449.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 12 Jul 2010 10:21:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Coumadin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Coumadin Tablets]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Subpotent]]></REASON>
	<COMPANY><![CDATA[Bristol-Myers Squibb]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm218864.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 08 Jul 2010 14:34:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Benadryl; Tylenol; Motrin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Over the counter (OTC) products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Uncharacteristic smell caused by the presence of trace amounts of a chemical called 2,4,6-tribromoanisole (TBA)]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm218437.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 25 Jun 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Magic Power Coffee]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Contains undeclared hydroxythiohomosildenafil, an analog of Sildenafil]]></REASON>
	<COMPANY><![CDATA[INZ Distributors Inc./Magic Power Coffee Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm217482.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 24 Jun 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Sinex]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Nasal Spray]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may not meet package expiration date]]></REASON>
	<COMPANY><![CDATA[The Procter &amp; Gamble Company]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm217376.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 15 Jun 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Benadryl; Tylenol]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Over the counter (OTC) products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Uncharacteristic smell caused by the presence of trace amounts of a chemical called 2,4,6-tribromoanisole (TBA)]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm215921.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 02 Jun 2010 14:40:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Sagent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[ondansetron injection in 5% dextrose 32mg / 50 mL]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[foreign material and non-sterility]]></REASON>
	<COMPANY><![CDATA[Sagent Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm214244.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 01 Jun 2010 13:29:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Claris]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[particulate matter]]></REASON>
	<COMPANY><![CDATA[Claris Lifesciences]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm214220.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 28 May 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[PediaCare]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[PediaCare Products: Multi-Symptom Cold, Long Acting Cough,  Decongestant, and Allergy and Cold]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain particulate matter]]></REASON>
	<COMPANY><![CDATA[Blacksmith Brands, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm214005.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 27 May 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hospira]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Propofol Injectable Emulsion 1% and Liposyn™ (Intravenous Fat Emulsion) products which include Liposyn II 10%, Liposyn II 20%, Liposyn III 10%, Liposyn III 20%, and Liposyn III 30%]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[may contain particulate matter]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm213880.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 17 May 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[no brand name]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Hylenex (hyaluronidase human injection)]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[glass contamination]]></REASON>
	<COMPANY><![CDATA[Baxter International Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm213012.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 12 Apr 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[72 Hours (all strengths), Amour Again for Him, Arousin, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient/unapproved drug]]></REASON>
	<COMPANY><![CDATA[Atlas Operations, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm208537.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 02 Apr 2010 16:48:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Stud Capsule]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient/unapproved drug]]></REASON>
	<COMPANY><![CDATA[Kanec USA Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm207479.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 02 Apr 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Camolyn, Fisiolin]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Eye and Nasal Drops]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Sterility]]></REASON>
	<COMPANY><![CDATA[US Oftalmi]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm207735.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 30 Mar 2010 15:05:00 -0400</DATE>
	<BRAND_NAME><![CDATA[MasXtreme]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient/unapproved drug]]></REASON>
	<COMPANY><![CDATA[Natural Wellness, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm206759.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 17 Mar 2010 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Cleviprex]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Cleviprex (clevidipine butyrate) injectable emulsion]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Particulate matter]]></REASON>
	<COMPANY><![CDATA[The Medicines Company]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm204997.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 15 Jan 2010 15:48:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Advanced Muscle, Anabolic Formulation, Anabolic Xtreme, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplements]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared drug ingredient/unapproved drug]]></REASON>
	<COMPANY><![CDATA[MuscleMaster.com, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm197824.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 15 Jan 2010 10:38:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Motrin, Tylenol, Benedryl, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drug Products]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Off-odor]]></REASON>
	<COMPANY><![CDATA[McNeil Consumer Healthcare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2010/ucm197746.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 18 Dec 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Tylenol]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Presence of 2,4,6-tribromoanisole]]></REASON>
	<COMPANY><![CDATA[McNeil-PPC, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm195690.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 16 Dec 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Cleviprex]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulate matter]]></REASON>
	<COMPANY><![CDATA[The Medicines Company]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm194555.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 11 Dec 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Aspire One, Sex Enhancer, Staminil]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient]]></REASON>
	<COMPANY><![CDATA[Atlas Operations, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm194074.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 08 Dec 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Alka-Seltzer]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Mislabeled]]></REASON>
	<COMPANY><![CDATA[Bayer HealthCare]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm193409.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 19 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Vicks]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[B. cepacia]]></REASON>
	<COMPANY><![CDATA[The Procter &amp; Gamble Company]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm191416.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 12 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Pai You Guo]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient]]></REASON>
	<COMPANY><![CDATA[GMP Herbal Products, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm190403.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 12 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Bromodrol, Dual Action Grow Tabs, Mass Tabs, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient]]></REASON>
	<COMPANY><![CDATA[IDS Sports]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm190446.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 09 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Rockhard Weekend]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient]]></REASON>
	<COMPANY><![CDATA[RockHard Laboratories]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm191001.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 06 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Liposyn]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[May contain particulate matter]]></REASON>
	<COMPANY><![CDATA[Hospira, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm189564.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 03 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Adverse reaction]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm188954.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 03 Nov 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Black China Labs, Advanced Muscle Science, Engineered Sports Technology, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient]]></REASON>
	<COMPANY><![CDATA[Bodybuilding.com]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm188929.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 20 Oct 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[American Regent]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Adverse reaction]]></REASON>
	<COMPANY><![CDATA[American Regent]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm187434.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 21 Aug 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Steam]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient, Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Nutracoastal Trading LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm179964.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK>
	</PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 13 Aug 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Barr Laboratories, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect ingredient levels]]></REASON>
	<COMPANY><![CDATA[Barr Laboratories, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm177321.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 28 Jul 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[S-DROL]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient, Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Nutracoastal Trading LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm174226.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 23 Jul 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Steam]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient, Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Nutracoastal Trading LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm174229.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 15 Jul 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Slimbionic, One Weight Loss Pill, SlimDemand, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient]]></REASON>
	<COMPANY><![CDATA[Young You Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm172478.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 13 Jul 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Brookstone]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Acetaminophen Drops]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect ingredient levels]]></REASON>
	<COMPANY><![CDATA[Brookstone Pharmaceuticals, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm171780.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 22 May 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Fun Express, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Face Paint]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Adverse reaction]]></REASON>
	<COMPANY><![CDATA[Fun Express, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm161554.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 11 May 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Caraco]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect ingredient levels]]></REASON>
	<COMPANY><![CDATA[AS Medication Solutions, LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm150734.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Thu, 07 May 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Hydroxycut]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Adverse reaction]]></REASON>
	<COMPANY><![CDATA[Iovate Health Sciences USA, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm150313.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 29 Apr 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Personal Care]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Personal Care Product]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Adverse reaction]]></REASON>
	<COMPANY><![CDATA[Personal Care Products]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm143437.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 20 Apr 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Advent Pharma, Neilgen Pharma]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Unapproved drug]]></REASON>
	<COMPANY><![CDATA[Neilgen Pharma Inc., Advent Pharmaceutical]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm136552.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 20 Apr 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[ProSlim, 3 Days Fit, Eight Factor Diet, more]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient, Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Universal ABC Beauty Supply International, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm136918.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 13 Apr 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Influend]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect ingredient levels]]></REASON>
	<COMPANY><![CDATA[ION Labs Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm134662.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 31 Mar 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Caraco]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect ingredient levels]]></REASON>
	<COMPANY><![CDATA[Caraco Pharmaceutical Labratories, Ltd.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm128443.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Mon, 23 Mar 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Watson Pharmaceuticals, Inc.]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Incorrect ingredient levels]]></REASON>
	<COMPANY><![CDATA[Watson Pharmaceuticals, Inc.]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm129032.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Fri, 20 Mar 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[DAYTRANA]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Medical patch]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Manufacturing problem]]></REASON>
	<COMPANY><![CDATA[Shire plc]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm128798.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 11 Mar 2009 00:00:00 -0400</DATE>
	<BRAND_NAME><![CDATA[Zencore Plus]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Dietary Supplement]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[Undeclared ingredient, Unapproved new drug]]></REASON>
	<COMPANY><![CDATA[Bodee LLC]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm128422.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Tue, 03 Feb 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[ETHEX Corporation]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[cGMPs]]></REASON>
	<COMPANY><![CDATA[ETHEX Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm128537.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
<PRODUCT>
	<DATE>Wed, 28 Jan 2009 00:00:00 -0500</DATE>
	<BRAND_NAME><![CDATA[Ther-RX Corporation]]></BRAND_NAME>
	<PRODUCT_DESCRIPTION><![CDATA[Drugs]]></PRODUCT_DESCRIPTION>
	<REASON><![CDATA[cGMPs]]></REASON>
	<COMPANY><![CDATA[Ther-RX Corporation]]></COMPANY>
	<COMPANY_RELEASE_LINK>http://www.fda.gov/Safety/Recalls/ArchiveRecalls/2009/ucm128972.htm</COMPANY_RELEASE_LINK>
	<PHOTOS_LINK></PHOTOS_LINK>
</PRODUCT>
</RECALLS_DATA>

