Recalls of Products Intended for Health, page 3

Product Recalls

Thu, 08 Jul 2010

McNeil Consumer Healthcare Announces Voluntary Recall of Certain Over-The-Counter (OTC) Products in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad, Tobago, and Jamaica.

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling 21 lots of over-the-counter medicines. The lots involved are sold in the United States, Fiji, Guatemala, Dominican Republic, Puerto Rico, Trinidad & Tobago, and Jamaica.

http://www.fda.gov/Safety/Recalls/ucm218437.htm

Tue, 13 Jul 2010

Bristol-Myers Squibb Initiates a Nationwide Voluntary Recall of Coumadin (R) 1 mg Tablet Blister Packs

Bristol-Myers Squibb initiates a voluntary recall of 3 lots of physician sample blister packs of
Coumadin® 1 mg tablets and 5 lots, of Coumadin 1 mg tablet hospital unit dose (HUD) blister packs. The following lot numbers are included in this recall: Physician Sample Blister Packs: Lot# 9A48931A, 9A48931B, 9A48931C, expiration January 2012; HUD Blister Pack: Lot# 8F34006B, 8K44272A, 8K46168A, 9F44437A and 9K58012B with expiry dates between June 2011 and November 2012…

http://www.fda.gov/Safety/Recalls/ucm218864.htm

Fri, 16 Jul 2010

J & H Besta Corp. Issues a Voluntary Nationwide Recall of Slim- 30 Herb Supplement Found to Contain an Undeclared Drug Ingredient
J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Slim-30 Herb Supplement distributed by the company was found to contain undeclared N-Desmethyl Sibutramine and traces of Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved this product, therefore the safety and effectiveness of the product is unknown.

http://www.fda.gov/Safety/Recalls/ucm219449.htm

Fri, 16 Jul 2010

D & M Smoked Fish, Inc. Issues an Allert on Uneviscerated Schmaltz Herring

D & M Smoked Fish, Inc. located in Queens, New York, is recalling Haifa brand vacuum packaged Schmaltz Herring with the lot number 168, because the product was found to be uneviscerated. The
lot being recalled is a product of Norway, individually vacuum-packed in clear plastic pouches with lot # 168 & Sell by date of 7/20/10 indicated on the label and distributed through food retailers in the NY area.

http://www.fda.gov/Safety/Recalls/ucm219439.htm

Tue, 20 Jul 2010

Good Health, Inc. Issues a Nationwide Voluntary Recall of Product Marketed as Dietary Supplement

Good Health, Inc. announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement Vialipro for sexual enhancement sold under the Lot Numbers listed below. This product is currently being sold as a dietary supplement throughout the U.S. Good Health, Inc. is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that a lab analyses found that the product tested from certain batches of Vialipro contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED) making this product an unapproved drug. The active drug ingredient is not listed on the product label.

http://www.fda.gov/Safety/Recalls/ucm219558.htm

Thu, 22 Jul 2010

J & H Besta Corp. Issues a Voluntary Nationwide Recall of Joyful Slim Herb Supplement Found to Contain an Undeclared Drug Ingredient
J & H Besta Corp. of Hicksville, NY, has been informed by the Food and Drug Administration (FDA) that FDA lab analysis of Joyful Slim Herb Supplement distributed by the company was found to contain undeclared Desmethyl Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The FDA has not approved this product, therefore the safety and effectiveness of the product is unknown.

http://www.fda.gov/Safety/Recalls/ucm219962.htm

Mon, 26 Jul 2010

Airgas South Initiates Precautionary Voluntary Recall of Medical Gas Products at Chattanooga, TN
Facility
Airgas South, Inc., a distributor of industrial, medical, and specialty gases, today announced an expanded voluntary recall of medical gas products filled at its Chattanooga, Tennessee facility. The recall is being initiated as a precautionary measure because these products may have been
manufactured under conditions that did not sufficiently comply with current Good Manufacturing
Practices (cGMPs). These practices help assure that drug products meet required quality standards for quality, purity and potency.

http://www.fda.gov/Safety/Recalls/ucm220227.htm

Tue, 27 Jul 2010

P&G Recalls Two Lots of Prescription Renal Diet Cat Food due to a Possible Health Risk
The Procter & Gamble Company (P&G) (NYSE:PG), is voluntarily recalling two specific lots of its
prescription renal dry cat food as a precautionary measure, as it has the potential to be contaminated with salmonella. The products included are listed at:

http://www.fda.gov/Safety/Recalls/ucm220204.htm

Tue, 27 Jul 2010

Voluntary Recall of PreserVision® Eye Vitamin AREDS 2 Formula in the United States
Bausch + Lomb is conducting a voluntary recall of its PreserVision® Eye Vitamin AREDS 2 Formula with Omega 3 soft gels, only available within the United States. Bausch + Lomb chose to initiate this recall based on a small number of reports predominantly within a specific age group, age 70 and older, who reported difficulty swallowing or a choking sensation when taking the soft gel.

http://www.fda.gov/Safety/Recalls/ucm220353.htm

Wed, 28 Jul 2010

Biggers & Callaham, Llc Dba Mice Direct Recalls Frozen Reptile Feed Because Of Possible Health Risk Biggers & Callaham LLC., D/B/A Mice Direct of Cleveland Georgia is recalling frozen reptile feed
(mice, rats, chicks), because it has the potential to be contaminated with Salmonella. Salmonella
can affect animals and there is risk to humans from handling contaminated pet products.

http://www.fda.gov/Safety/Recalls/ucm220367.htm

Thu, 29 Jul 2010

Nutraloid Labs Inc. Conducts Voluntary Nationwide Recall of Two Dietary Supplements Found to Contain Undeclared Drug Ingredient Nutraloid Labs Inc. announced today that it is conducting a voluntary nationwide recall of two dietary supplement products sold under the names: ejaculoid XXTREME and stimuloid II. Nutraloid Labs Inc. has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis of ejaculoid XXTREME, Lot 79935, and stimuloid II, Lot 79936, by the FDA found that the
products contain sulfoaildenafil, similar in structure to Sildenafil.

http://www.fda.gov/Safety/Recalls/ucm220601.htm

Sat, 07 Aug 2010

EZVille, Ltd. Issues a Voluntary Nationwide Recall of Revivexxx® Extra Strength Found to Contain an
Undeclared Drug Ingredient

EZVille, Ltd. of Ronkonkoma, NY, has been informed by the US Food and Drug Administration (FDA)
that FDA lab analysis of Revivexxx® Extra Strength distributed by the company was found to contain
undeclared tadalafil. Tadalafil is an FDA-approved drug for the treatment of male Erectile
Dysfunction (ED), making Revivexxx® Extra Strength an unapproved drug.

http://www.fda.gov/Safety/Recalls/ucm221663.htm

Sat, 07 Aug 2010

EZVille, Ltd. Issues a Voluntary Nationwide Recall of Solo Slim® Found to Contain an undeclared Drug Ingredient

EZVille, Ltd. of Ronkonkoma, NY, has been informed by the Food and Drug Administration (FDA) that
FDA lab analysis of Solo Slim® distributed by the company was found to contain an undeclared drug
ingredient. Solo Slim® was found to contain Didesmethyl Sibutramine. Sibutramine is an FDA-approved
drug used as an appetite suppressant for weight loss. The FDA has not approved Solo Slim®,
therefore the safety and effectiveness of the product is unknown.

http://www.fda.gov/Safety/Recalls/ucm221660.htm

Tue, 10 Aug 2010

Novacare LLC Conducts Voluntary Nationwide Recall of Products Found to Contain Undeclared Drug
Ingredient

Novacare LLC announced today that it is conducting a voluntary nationwide recall of products sold
under the following names: 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, and Zilex (with Golden Spear). Novacare LLC has been informed by
representatives of the Food & Drug Administration (FDA) that the products appear to contain
sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male
Erectile Dysfunction.

http://www.fda.gov/Safety/Recalls/ucm221958.htm

Fri, 13 Aug 2010
Wright County Egg Conducts Nationwide Voluntary Recalls of Shell Eggs Because of Possible Health
Risk

The following statement was released by officials of Wright County Egg regarding the US Food and Drug Administration’s (FDA) on-farm records review and egg testing for Salmonella. Wright County Egg of Galt, Iowa is voluntarily recalling specific Julian dates of shell eggs produced by their farms because they have the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

http://www.fda.gov/Safety/Recalls/ucm222501.htm

Wed, 18 Aug 2010

Glow Industries, Inc., Perrysburg, OH, announced today that it is initiating a voluntary nationwide
recall of the company’s product sold under the name of Mr. Magic Male Enhancer from Don Wands. Glow
Industries, Inc. is conducting this voluntary recall after being informed by the Food and Drug
Administration (FDA) that lab analysis has found the Mr. Magic Male Enhancer from Don Wands
capsules to contain Hydroxythiohomosildenafil and Sulfoaildenafil, an analogue of Sildenafil, an
FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making Mr. Magic Male
Enhancer an unapproved new drug. These active ingredients are not listed on the product label.
Product manufactured containing lot numbers 9041401, 251209 and 8121904 are included in this
recall…

http://www.fda.gov/Safety/Recalls/ucm223082.htm

Product Recalls – 2 – Page 3 – 4 – Last Page 5

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