The U.S. Food and Drug Administration today announced that the U.S. District Court for the Southern District of Texas entered a consent decree of permanent injunction against Deltex Pharmaceuticals Inc., of Rosenberg, Texas, its president, Kabir Ahmed, and vice president, Mohidur R. Khan.
The consent decree permanently prohibits/stops the company, Ahmed, and Khan from manufacturing and distributing drug products until Deltex’s manufacturing operations and products are in compliance with federal law and the terms of the consent decree.
Barry Callebaut USA LLC Issues Allergen Alert on Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips
Barry Callebaut USA LLC is conducting a voluntary recall on its product sold by Kroger Stores under the brand “Kroger Value Semi Sweet Chocolate Chips”, 12 oz., UPC Code is 11110–86603 as the product may contain undeclared milk protein.
All “Best By” dates ending in 2012 are affected by this voluntary recall.
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Genentech Informs Customers Of Important Information About Triad Groups
Genentech, Inc., a member of
the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), has become aware of the market
recall of Triad Groupʼs alcohol prep pads, alcohol swabs, and alcohol swabsticks
manufactured by Triad in the United States and marketed under various brand names.
The Triad Group alcohol prep
pads are co-packaged and distributed with Genentech medicines, Boniva Injection,
Fuzeon, Nutropin A.Q. Pen, Pegasys, and TNKase to customers in the United States.
McNeil Consumer Healthcare Initiates Voluntary Recall Of Certain Over-The-Counter (OTC) Products
– In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc. is voluntarily recalling, at the wholesale level, certain lots of TYLENOL® 8 Hour, TYLENOL® Arthritis Pain, and TYLENOL® upper respiratory products, and certain lots of BENADRYL®, SUDAFED PE®, and SINUTAB® products distributed in the United States, the Caribbean, and Brazil. These products were manufactured at the McNeil plant in Fort Washington, PA prior to April 2010, when production at the facility was suspended.
FDA seeks to halt processing, distribution at New York juice company
At the request of the U.S. Food and Drug Administration, the U.S. Department of Justice today filed a complaint for permanent injunction against a Jamaica, N.Y.-based beverage company to prevent it from processing and distributing juice and other products. (DSK)
MS Fish Corp Issues Alert On Listeria In
MS FISH CORP 808 ALABAMA AVE, BROOKLYN, NY 11207 is recalling Ossie’s Schmaltz Herring due to Listeria monocytogenes contamination.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail, or elderly people and others with weakened immune systems.
Candy Dynamics Recalls Toxic Waste® brand Nuclear Sludge® Chew Bars
Circle City Marketing and Distributing doing business as Candy Dynamics, Indianapolis, IN, is issuing a voluntary recall of all Toxic Waste® brand Nuclear Sludge® Chew Bars, all flavors, Net wt. 0.7 oz (20 g) package. The product is imported from Pakistan.
Barry Callebaut USA LLC Issues Allergen Alert on Potential Undeclared Milk Protein in Kroger Value Semi Sweet Chocolate Chips
Barry Callebaut USA LLC is conducting a voluntary recall on its product sold by Kroger Stores under the brand “Kroger Value Semi Sweet Chocolate Chips”, 12 oz., UPC Code is 11110–86603 as the product may contain undeclared milk protein.
The “Best By” date is found printed in black on the end of the back of the bag.
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FDA limits acetaminophen in prescription combination products; requires liver toxicity warnings
Agency strategy caps maximum at 325 milligrams to reduce risk of liver toxicity.
U.S. Marshals seize dental devices from Florida manufacturer
U.S. Marshals, acting under a court order sought by the U.S. Food and Drug Administration, today seized all dental devices from Rite-Dent Manufacturing Corporation, located in Hialeah, Fla. (DSK)