Nestlé Purina PetCare Company (NPPC) is voluntarily recalling approximately 870 bags of dry cat food shipped to Colorado, Idaho and Oregon. This is being done as a precautionary measure, as the product has the potential to be contaminated with Salmonella.
JFC International Inc. Issues Allergy Alert Due To Undeclared Milk Protein in UCC and Taitan Instant Drink Mix Products
JFC International, Inc. of Los Angeles, CA is recalling all UCC and Taitan Instant Drink Mix because they contain undeclared milk protein. People who have an allergy or severe sensitivity to milk may run the risk of serious or life-threatening allergic reactions if they consume these products.
Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recall of Four Lots of Butalbital, Acetaminophen, and Caffeine Tablets, USP 50mg/325mg/40mg and Four Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg
Qualitest Pharmaceuticals today issued a voluntary nationwide retail level recall of Butalbital, Acetaminophen, and Caffeine Tablets USP, 50mg/325mg/40mg, and Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg. This recall was initiated because an individual bottle of Butalbital, Acetaminophen, and Caffeine Tablets USP, 50mg/325mg/40mg, 500 count was found incorrectly labeled with a Hydrocodone Bitartrate and Acetaminophen Tablets, USP 7.5mg/500mg, 1000 count label, printed with Lot Number C0590909B.
Endo Pharmaceuticals Issues Voluntary, Nationwide Recall of Two Lots of Endocet® (Oxycodone/Acetaminophen, USP) Tablets, 10 MG / 325 MG
Endo Pharmaceuticals today issued a voluntary nationwide consumer level recall of Endocet® (oxycodone/acetaminophen, USP) Tablets, 10 mg/325 mg 100 count bottles, NDC 60951-712-70, Lot # 402415NV and #402426NV. One bottle from each lot of Endocet® (oxycodone/acetaminophen, USP) Tablets, 10 mg/325 mg, Lot # 402415NV and # 402426NV, NDC 60951-712-70, 100 count bottles, was found to contain some Endocet® 10 mg/650 mg Tablets, which are identifiable by their larger size, and different shape and markings.
Eagle Produce, LLC Recalls Cantaloupe Due To Possible Health Risk
Scottsdale, AZ – Eagle Produce, LLC of Scottsdale, Arizona has announced a limited recall of certain cantaloupes shipped from Arizona to upstate New York
in late May, due to their potential to be contaminated with salmonella. Although no illnesses
have been reported, Eagle Produce has voluntarily decided to recall the potentially affected shipments, which were sold at Sam’s Club between June 2 and June 17, 2011. Sam’s Club
has withdrawn all cantaloupes from the Clubs and sent a notification to Members that bought these melons from Clubs served by the Johnstown, NY and Pottsville, PA
distribution centers.
Nature Relief is Conducting a Voluntary Recall of Nature Relief Instant Wart and Mole Remover
Nature Relief is voluntarily recalling Nature Relief Instant Wart and Mole Remover. Consumers are advised to discontinue use and immediately dispose of any used or unused portions of the product.
FDA modifies dosing recommendations for Erythropoiesis-Stimulating Agents
The U.S. Food and Drug Administration today recommended more conservative dosing guidelines for Erythropoiesis-Stimulating Agents (ESAs) when used to treat anemia in patients with chronic kidney disease (CKD) because of the increased risks of cardiovascular events such as stroke, thrombosis, and death.
Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Italian Blend Salads
Dole Fresh Vegetables is voluntarily recalling 2,880 cases of DOLE® Italian Blend salad with Use-by Date of June 19, 2011, UPC code 7143000819 and Product Codes 0049A157201A, 0049A157201B, 0049A157202A, 0049A157202B, 0686A157202A, 0686A157202B and 442 cases of Kroger Fresh Selections Italian Style Blend salad with Use-by-Date of June 19, 2011, UPC code 1111091045 and Product Codes A157201A & A157201B, due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials.
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FDA provides updated safety data on silicone gel-filled breast implants
The U.S. Food and Drug Administration released a report today updating the clinical and scientific information for silicone gel-filled breast implants, including preliminary safety data from studies conducted by the manufacturers as a condition of their November 2006 approval.
FDA: Maryland food manufacturer enters into consent decree
The U.S. Food and Drug Administration announced that Sungwon Inc of Columbia, a Columbia, Md., corporation, and the company’s president, Sang Ja Lee, have signed a consent decree of permanent injunction.