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FDA: Recalls
Recall Information from FDA
Updated: 2 hours 7 min ago
INZ Distributors Inc./Magic Power Coffee Inc. Conducts a Voluntary Nationwide Recall of Magic Power Coffee Dietary Supplement
INZ Distributors Inc./Magic Power Coffee Inc. of Brooklyn, NY announced today that it is conducting a voluntary nationwide recall of the dietary supplement product sold under the name, Magic Power Coffee. The Company has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis of one lot of the product by the FDA found that the product contains undeclared hydroxythiohomosildenafil, similar in structure to Sildenafil, an FDA-approved drug used for the treatment of male Erectile Dysfunction (ED), making Magic Power Coffee an unapproved drug.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Pure Base Distrbution Issues Allergy Alert on Undeclared Milk and Wheat in "Pure Base Garlic Spread - Concentrate" and "Pure Base Garlic Spread - Ready to Spread"
Pure Base Distribution, LLC of Ontario, CA is recalling its 4 ounce bottles of "Pure Base Garlic Spread - Concentrate" and 7 ounce bottles of "Pure Base Garlic Spread - Ready to Spread" items because they may contain undeclared milk and wheat. People who have allergies to milk and/or wheat run the risk of serious or life-threatening allergic reaction if they consume these products. If you or a member of your household is allergic to milk or wheat products, do not consume these products, but return them to your retailer for a full refund.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
P&G Voluntarily Recalls 4 Hour Decongestant Nasal Spray in the United States
The Procter & Gamble Company (NYSE:PG) announced today it is voluntarily recalling its 4-Hour Decongestant Nasal Spray. The product was distributed nationwide in the United States.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Kellogg Company Voluntarily Recalls Select Packages of Kellogg's® Corn Pops®, Kellogg's® Honey Smacks®, Kellogg's® Froot Loops® and Kellogg's® Apple Jacks®
Working in consultation with the United States Food and Drug Administration (FDA), Kellogg Company (NYSE:K) is implementing a voluntary recall of certain breakfast cereals due to an uncharacteristic off-flavor and smell coming from the liner in the package. Only products with the letters "KN" following the Better If Used Before Date are included in the recall.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Lancaster Foods, LLC Voluntarily Recalls Fresh Spinach with Best Enjoyed By Dates of June 19 to June 27, 2010 Due to Possible Health Risk
Lancaster Foods, LLC is voluntarily recalling fresh Spinach with the Best Enjoyed By dates of 19 JUN 10 through 27 JUN 10 sold under the brand names Krisp-Pak, Lancaster Fresh, Giant, and America's Choice because they could be contaminated with Listeria monocytogenes. The recall extends only to products with this Use-by Date or Product Code and sold in the following states: New Jersey, Delaware, Pennsylvania, Maryland, North Carolina, and Virginia...
Categories: NEWS: U.S. Food and Drug Administration (FDA)
United Pet Group Voluntarily Recalls Pro-Pet Adult Daily Vitamin Supplement for Dogs Because of Possible Salmonella Health Risk
United Pet Group, Cincinnati, Ohio is voluntarily recalling all unexpired lots of its PRO-PET ADULT DAILY VITAMIN Supplement tablets for Dogs due to possible Salmonella contamination. The Food and Drug Administration is aware of this recall.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Portland Shellfish Company Expands Recall to Include Meat Without Feet Label, Lobster Claw and Knuckle Meat, because of Possible Health Risk
Portland Shellfish Company, Inc. is expanding this voluntarily recall to include the Meat Without Feet private label food service (2 Lb bags), pack of ready to eat frozen lobster claw and knuckle meat. Lot 13310, as recent tests show the product has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Rich Products Corporation announces nationwide voluntary recall of Allen Bavarian Crème Filling due to undeclared allergens in product
Rich Products Corporation on June 18, 2010 voluntarily recalled its Allen Bavarian Crème Filling (product code 02881) with Production codes 11870137F21, F-22, F-23, F-24, F-25, because the product may contain undeclared pecans, milk, and coconut. People who have an allergy or severe sensitivity to these ingredients run the risk of serious or life-threatening allergic reaction if they consume these products.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Natural Balance Pet Foods, Inc. announces a voluntary recall of Natural Balance Sweet Potato & Chicken Dry Dog Food Due to a Possible Health Risk
Natural Balance Pet Foods, Inc., of Pacoima, CA, announces a voluntary recall of Natural Balance Sweet Potato & Chicken Dry Dog Food with the “Best By” date of June 17, 2011, in 5-lb. and 28-lb. bags because it has the potential to be contaminated with Salmonella.
No illnesses have been reported to date.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Kent Nutrition Group, Inc. Conducts Nationwide Voluntary Recall of Kent Feeds Swine Products
Kent Nutrition Group, Inc. (KNG) is voluntarily recalling some Kent Feeds swine feed products due to insufficient vitamin D levels in premixes it purchased from Tri Ag Supply, Inc. that were used in those swine feed products. The recall is being implemented in order to prevent health problems in swine consuming feed products where there is a vitamin D3 deficiency.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Mcneil Consumer Healthcare Recalls Four Product Lots of Benadryl® Allergy Ultratab™ Tablets, 100 Count, and One Product Lot of Extra Strength Tylenol® Rapid Release Gels, 50 Count
Fort Washington, PA (June 15, 2010) – McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling five product lots as an addition to the list of products included in the company’s January 15th, 2010 product recall. The additional lots involved are four product lots of BENADRYL® ALLERGY ULTRATAB™ TABLETS, 100 count, sold in the U.S.; and one product lot of EXTRA STRENGTH TYLENOL® Rapid Release Gels, 50 count sold in the U.S., Trinidad and Tobago, Bermuda, and Puerto Rico (FULL RECALLED PRODUCT LIST BELOW).
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Portland Shellfish Company Recalls Cooked, Frozen Claw Island Brand, Craig’s All Natural Brand And Inland Ocean Brand Lobster Claw And Knuckle Meat Because Of Possible Health Risk
Portland Shellfish Company, Inc. is voluntarily recalling the following brands of cooked, ready to eat fresh or frozen lobster meat: Portland Shellfish Co. Inc brand, Claw island, Craig’s All Natural, and Inland Ocean cooked, fresh or frozen lobster claw and knuckle meat as recent tests show the product has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Sirob Imports Issues Alert on Undeclared Sulfites in Strawberry Farms Sun Dried Tomatoes
Sirob Imports, Inc. of Lindenhurst, NY, is recalling 16 oz vacuum packed bags of Strawberry Farm Sun Dried Tomatoes because they contain undeclared sulfites. Consumers who have severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Kroger Recalls Select Containers of Deluxe Chocolate Paradise Ice Cream for Undeclared Allergen
The Kroger Co. said today it is recalling select containers of Kroger Deluxe Chocolate Paradise Ice Cream sold in 17 states because it may contain tree nuts not listed on the label. Customers should return the product to stores for a full refund or replacement.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Bimbo Bakeries USA, Inc. Announces Recall of Bimbo Soft White Bread Due To Undeclared Milk
Bimbo Bakeries USA, Inc. is recalling Bimbo brand Soft White Bread (1 lb. 4 oz. or 567 grams) sold in California, Idaho, Oregon and Washington because it may contain undeclared milk. People who have an allergy to milk run the risk of life threatening or serious allergic reaction if they consume the product.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Domega NY International Co., LTD Issues Allergy Alert on Undeclared Egg in Fuma Custard Pie
DOMEGA NY INTERNATIONAL CO. LTD 4820 2nd AVE BROOKLYN NY 11232 is recalling FUMA CUSTARD PIE because it may contain undeclared eggs. Consumers who are allergic to eggs may run the risk of serious or life-threatening allergic reactions if they consume this product.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
P&G Recalls Specific Canned Cat Foods Due to Low Levels of Thiamine (Vitamin B1)
The Procter & Gamble Company (P&G) (NYSE:PG) is voluntarily recalling specific lots of its Iams canned cat food in North America as a precautionary measure. Diagnostic testing indicated that the product may contain insufficient levels of thiamine (Vitamin B1), which is essential for cats. Cats that were fed these canned products as their only food are at greater risk for developing signs of thiamine deficiency.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Defibtech Announces a Voluntary Recall of DBP-2800 Battery Packs used in the Lifeline AED<sup>® </sup>and ReviveR AED<sup>TM</sup>
Defibtech, LLC, is
initiating a voluntary recall of 5,418 DBP-2800 Battery Packs used in the Lifeline AED®
and ReviveR AEDTM (semi-automatic external defibrillators). This recall affects all DBP-
2800 Battery Packs shipped prior to June 4, 2007. In rare instances, when the AED is
used with an affected battery pack, the AED may falsely detect an error condition during
charging for a shock, then cancel charge and not provide therapy. Defibtech determined
the need for this recall after learning of four reports from end users of this malfunction
during patient use.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
West-Ward Pharmaceuticals Recalls Ondansetron in 5% Dextrose Injection And Metronidazole Injection, USP Bags Due To Possible Health Risk
West-Ward Pharmaceuticals Inc., of Eatontown, NJ, is voluntarily recalling all lots of Claris LifeSciences Inc. manufactured Ondansetron in 5% Dextrose Injection, supplied in 32mg/50mL Single-Use Plastic Bag Containers and Metronidazole Injection 500mg/100ml USP in Flexible IV Plastic Bag Containers. Claris recently received reports of the presence of floating matter and non-sterility in Ondansetron and Metronidazole. Non-sterile products administered intravenously may cause infections which could be fatal especially in patients who are immuno-compromised.
Categories: NEWS: U.S. Food and Drug Administration (FDA)
Pfizer Initiates a Nationwide Voluntary Recall of All Lots of Metronidazole Injection, Ciprofloxacin Injection, and Ondansetron Injection Bags Made by Claris Lifesciences Due to Non-Sterility
Pfizer Inc is voluntarily recalling Metronidazole, Ciprofloxacin and Ondansetron IV Products due to the presence of floating matter and non-sterility discovered by the manufacturer Claris Laboratories. Non-sterility of a product administered via the intravenous route has the potential to result in infections, which could be fatal, especially in patients who are immunocompromised. Metronidazole and Ciprofloxacin injections are intravenous antibiotics used to treat infections.
Categories: NEWS: U.S. Food and Drug Administration (FDA)