– Fresh Express is voluntarily recalling 2,825 cases of Veggie Lovers Salad with a Product Code of I208 and Use-by Date of August 10, 2010 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. No other Fresh Express salads are included in the recall. No illnesses have been reported in association with the recall.
Ikaria® Recalls INOMAX® DS Drug-Delivery System
Ikaria, Inc. announced today that its INOMAX® DS drug-delivery systems in
the United States are being voluntarily recalled due to the potential failure of a pressure switch which may
have an impact on the administration of INOMAX® (nitric oxide) for inhalation to patients. This potential
failure was identified by Ikaria as part of its ongoing quality monitoring and review processes. This class I
recall is being conducted with the knowledge of the U.S. Food and Drug Administration (FDA).
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.
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.
South Bend Chocolate Company Announces Nationwide Recall of Bountiful Blend Chocolates Due to Undeclared Tree Nuts
The South Bend Chocolate Company, South Bend, Indiana, is recalling 174 1-lb bags of Bountiful Blend, a blend of chocolate covered mixed nuts and dried fruits, because it contains undeclared cashews, almonds, pecans, and Brazil nuts. People who have an allergy or severe sensitivity to cashews, pecans, almonds or Brazil nuts run the risk of serious or life-threatening allergic reaction if they consume this product.
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Product Recall – Eugenio Brezzi Truffle Puree
Optimus, Inc. d/b/a Marky’s, Miami, FL is announcing the voluntary recall of Engenio Brezzi Truffle Puree products imported from Italy. Consumers in possession of any of these products should return it for a full refund to the retail outlet where it was purchased.
Merrick Pet Care Recalls Texas Hold’ems 10 oz Bag (Item # 60016 Lot 10127 Best by May 6 2012) because of Possible Salmonella Health Risk
Merrick Pet Care, Inc. of Amarillo, Texas is extending its July 2,2010 recall of 100z “Beef Filet Squares for Dogs (Texas Hold’Ems)” pet treat (ITEM # 60016 LOT # 10084TL7 BEST BY MARCH 24, 2012) to also include 83 cases of “Texas Hold’ems” (ITEM # 60016 LOT # 10127 BEST BY MAY 6, 2012) because they have the potential to be contaminated with Salmonella. Salmonella can affect animals and there is risk to humans from handling contaminated pet products.
P&G Expands Voluntary Limited Recall of Specialized Dry Pet Foods Due to Possible Health Risk
The Procter & Gamble Company (P&G) (NYSE:PG) is voluntarily expanding its recall to include veterinary and some specialized dry pet food as a precautionary measure because it has the potential to be contaminated with salmonella. No salmonella-related illnesses have been reported.
KCB Issues Allergy Alert on Possible Eggs In "KCB No Eggs Added Cake Rusk 28oz"
Kashmir Crown Baking, LLC of Linden, NJ, is recalling its “KCB No Eggs Added Cake Rusk (28oz)” Cake Rusk, made to expire on February 8th, 2011, because it is possible that they may contain eggs. People who have allergies to eggs run the risk of serious or life-threatening allergic reaction if they consume this product.
Lundbeck Inc. Announces the Voluntary Nationwide Recall of Two Lots of NeoProfen® (ibuprofen lysine) Injection
– Lundbeck Inc. has voluntarily recalled two lots of NeoProfen® (ibuprofen lysine) Injection that failed to meet a visible particulate quality requirement. These two lots are the only lots currently available to prescribers and therefore the recall will result in a temporary drug shortage.