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

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.

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

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.

Chanel Recalls Silk Scarves and Garments Due to Violation of Federal Flammability Standard

The garments fail to meet the federal flammability standard for wearing apparel, posing a fire hazard to consumers.

Mini Stars Building Sets Recalled by Edushape Due to Choking Hazard

Plastic knobs can break from the center of the stars, posing a choking hazard to young children.

Mizuno USA Inc. Recalls Baseball and Softball Gloves Due to Presence of Mold

Some gloves were found to contain a variety of molds that could cause respiratory or other infections in individuals with chronic health problems, or in individuals who have impaired immune systems.

Dollar Tree Recalls Glass Votive Candle Holders Due to Fire and Laceration Hazards

The glass votive candle holders can shatter while in use, posing a fire and laceration hazard to consumers.

Viking Range Corporation Agrees to $450,000 Civil Penalty for Failing to Report Defective Refrigerators

The U.S.

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

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.

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

Fort Washington, PA – 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.

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

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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