Salsa Cycles Recalls Handlebar Stems Due to Fall Hazard
January 5, 2011
Name of Product: Salsa Handlebar Stems
Units: About 6,500 units
Importer: Salsa Cycles, a subsidiary of Quality Bicycle Products, of Bloomington, Minn.
Hazard: The handlebar stems can crack or break, posing a fall hazard to the rider.
Incidents/Injuries: Salsa Cycles has received one report of a handlebar stem breaking that resulted in minor injuries.
Ritedose Corp. Recalls 0.083% Albuterol Sulfate Inhalation Solution
January 4, 2011
The Ritedose Corporation is recalling 0.083% Albuterol Sulfate Inhalation Solution, 3 mL (in 25, 30, and 60 unit dose vials). This product is a prescription inhalation solution, administered via nebulization, for the treatment and maintenance of acute asthma exacerbations and exercise induced asthma in children and adults. This product is being recalled because the 2.5 mg/3 mL single use vials are embossed with the wrong concentration of 0.5 mg/ 3 mL and therefore, represents a potential significant health hazard. The following lot numbers manufactured by The Ritedose Corporation under NDC: 0591-3797-83, 0591-3797-30, and 0591-3797-60 are included in the recall: 0N81, 0N82, 0N83, 0N84, 0NE7, 0NE8, 0NE9, 0NF0, 0P12, 0P13, 0P46, 0P47, 0PF0, and 0S15. No other Albuterol formulations or products are included in this recall.
SPROUTERS NORTHWEST RECALLS CLOVER BECAUSE OF POSSIBLE SALMONELLA RISK
January 4, 2011
Sprouters Northwest is recalling all of its clover and clover mix products because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.
Winn Meats Co. Recalls Ground Beef Products Due to Mislabeling
January 4, 2011
Winn Meats Co. is recalling approximately 25,600 pounds of ground beef products that were improperly labeled and potentially adulterated, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The products’ labels include “For Cooking Only,” indicating that they are intended for further processing to apply a full lethality at a federally inspected establishment. Because the products were distributed to non-federally inspected establishments where it cannot be verified that sufficient further processing occurred to remove foodborne pathogens that could have been present, these products must be removed from commerce.
Bach Cuc Recalls Teriyaki Beef Jerky Products: Mislabeling Allergen
January 4, 2011
The products subject to recall include: [View Labels] 8-ounce packages of “BACH CÚC TERIYAKI BEEF JERKY.” 10-pound cases of “BACH CÚC TERIYAKI BEEF JERKY.”
Each product bears the establishment number “EST. 18995A” inside the USDA mark of inspection. The products subject to recall were produced between Jan. 2010 and Dec. 29, 2010. These products were distributed to retail establishments nationwide.
Pilgrim’s Pride Recalls Breaded Chicken Wing Products
January 4, 2011
Pilgrim’s Pride, a Boaz, Ala., establishment, is recalling approximately 180,000 pounds of breaded chicken wing products because they contain an undeclared allergen, egg, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. Egg is a known allergen, which is not declared on the label.
PRock Marketing Recalls All Weight Loss Formulas Due To Sibutramine
January 3, 2011
PRock Marketing LLC has been informed by the Food and Drug Administration (FDA) that the weight loss dietary supplements sold and marketed contains an undeclared drug ingredient. The FDA lab analysist of the dietary supplements found the Authentic Formula Fruta Planta to contain 15.4 mg of Sibutramine, a controlled substance that was withdrawn from the market in October 2010 for safety reasons. No illnesses or injuries have been reported to the company to date in connection with these products.
Cumberland Pharmaceuticals Recalls Acetadote Vials
January 2, 2011
Cumberland Pharmaceuticals Inc. announced today that it has implemented a recall of 6 lots of Acetadote® (acetylcysteine) Injection, the Company’s injectable treatment to prevent or lessen liver injury after ingestion of a potentially toxic quantity of acetaminophen. Cumberland informed the U.S. Food and Drug Administration (FDA) of its plans to voluntarily recall these lots of Acetadote as a precautionary measure based on observed particulate matter found in a very small number of vials. The source of the particulate matter was from the glass vial produced by a former supplier. The recall, which is not being undertaken on the basis of any known adverse medical events, affects a limited supply of product. “We are recalling certain lots manufactured by a previous packaging supplier as a precautionary measure, and believe the risk of any serious adverse medical events to be remote,” said A.J. Kazimi, Chief Executive Officer of Cumberland Pharmaceuticals. “As part of ongoing quality assessment, we switched to a new vial packaging supplier in August of 2009. Patient safety, as always, remains our highest priority, and we are committed to taking the necessary steps to proactively protect patients from the potential of any safety risks.”
Drive Total Energy Issues A Voluntary Recall Of Rock Hard Extreme And Passion Coffee Dietary Supplements
January 1, 2011
Drive Total Energy recalls Rock Hard Extreme and Passion Coffee Dietary Supplements. Drive Total Energy is conducting the voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analyses found that the products to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used in the treatment of male Erectile Dysfunction (ED), making these products unapproved new drugs. The active drug ingredient is not listed on the product label.
Sponsors
