Monday, February 6, 2012

Expanded Recall: Via Xtreme Ultimate Sexual Enhancer Dietary Supplement For Men Recall

July 15, 2011 by  
Filed under Product Recalls & Alerts

Global Wellness, LLC. Hollywood, FL is expanding its voluntary nationwide recall of Via Xtreme Ultimate Sexual Enhancer Dietary Supplement For Men to the consumer level to include lot A032111.

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Posh Bakery Issues Allergy Alert on Undeclared Eggs in Butter Mini Croissants and Chocolate Mini-Croissants

July 8, 2011 by  
Filed under Product Recalls & Alerts

Posh Bakery of Santa Clara, CA is recalling all its Butter Mini Croissants and Chocolate Mini-Croissants due to use of an egg wash that was undeclared on the product label. People who have allergies to eggs run the risk of serious or life-threatening reactions if they consume this product.

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Evergreen Fresh Sprouts, LLC Voluntarily Recalls Alfalfa Sprouts and Spicy Sprouts Because Of Possible Health Risk

July 1, 2011 by  
Filed under Product Recalls & Alerts

Moyie Springs, Idaho-Evergreen Fresh Sprouts, LLC announced a voluntary recall of Alfalfa Sprouts and Spicy Sprouts because it has the potential to be contaminated with Salmonella.

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McNeil Consumer Healthcare Announces Voluntary Recall Of One Product Lot Of TYLENOL ® Extra Strength Caplets 225 Count Distributed In The U.S.

June 29, 2011 by  
Filed under Product Recalls & Alerts

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling at the retail level one product lot (60,912 bottles) of TYLENOL ®, Extra Strength Caplets, 225 count bottles, distributed in the U.S. The recalled product was manufactured in February, 2009.

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McNeil Consumer Healthcare Announces Voluntary Recall Of One Product Lot Of TYLENOL ® Extra Strength Caplets 225 Count Distributed In The U.S.

June 29, 2011 by  
Filed under Product Recalls & Alerts

McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling at the retail level one product lot (60,912 bottles) of TYLENOL ®, Extra Strength Caplets, 225 count bottles, distributed in the U.S. The recalled product was manufactured in February, 2009.

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Risvold’s Salads Inc ISSUES ALLERGY ALERT ON UNDECLARED allergens in Seafood Salad and Seafood Pasta Salad

June 28, 2011 by  
Filed under Product Recalls & Alerts

Risvold’s Salads Inc of Gardena, CA is recalling seafood salad and seafood pasta salad, because it may contain undeclared milk, sunflower, sesame and soy. People who have an allergy or severe sensitivity to milk, sunflower, sesame and soy run the risk of serious or life-threatening allergic reaction if they consume these products.

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Nestlé Purina Recalls Limited Number of Dry Cat Food Bags Due to a Potential Health Risk (Shipped Only to Colorado, Idaho and Oregon)

June 27, 2011 by  
Filed under Product Recalls & Alerts

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.

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Nestlé Purina Recalls Limited Number of Dry Cat Food Bags Due to a Potential Health Risk (Shipped Only to Colorado, Idaho and Oregon)

June 27, 2011 by  
Filed under Product Recalls & Alerts

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.

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JFC International Inc. Issues Allergy Alert Due To Undeclared Milk Protein in UCC and Taitan Instant Drink Mix Products

June 27, 2011 by  
Filed under Product Recalls & Alerts

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.

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Qualitest Pharmaceuticals Issues Voluntary, Nationwide Retail Level Recall of Four Lots of Butalbital, Acetaminophen, and Caffeine Tablets, USP…

June 26, 2011 by  
Filed under Product Recalls & Alerts

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.

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