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  • Colorado Firm Recalls Ground Beef Products Due To Possible Salmonella Contamination
    King Soopers, Inc, of Denver, CO, is recalling approximately 466,236 pounds of ground beef products that may be linked to an outbreak of salmonellosis. The products subject to recall include: 1-pound chubs of (93/7) ground beef. Each package bears the identifying case code "69558." 1 - 1.25-lb. tray packs of (96/4) ground beef. Each package bea...
  • Polaris Recalls ATVs Due to Fire Hazard
    About 4,700 2009 Model Year Polaris All-Terrain Vehicles (ATVs) manufactured by Polaris Industries Inc., are being recalled because the valve assembly can fail in freezing temperatures, causing oil to leak into the exhaust system. This could pose a fire and burn hazard to the rider. The firm has received 6 reports of the valve assembly failing in free...
  • Fiesta Recalls Gas Grills Due to Fire, Burn Hazards
    Fiesta Gas Grills, of Dickson, TN, is recalling its Blue Ember Gas Grills, about 88,000 units in the United States and 25,000 units in Canada. The recall has been issued because the hose of the gas tank can get too close to the firebox and be exposed to heat, posing a fire hazard to consumers. Fiesta has received 161 reports of grill fires, resu...
  • Drager Stabilet Infant Warmer Lawsuit News and Legal Information
    Drager Medical Inc., has initiated a voluntary recall of Stabilet Infant Warmer models 200, 300, 1250, 1500, 200/3000, 2000, 2200/3200, 3000, and 3200. This action is in response to an event that took place in a neonatal unit of a hospital in Minnesota in 2008. ECRI conducted an investigation of the event and concluded that the likely cause was the St...
  • Nationwide Recall of Weight Loss Pills
    Young You Corporation has been informed by the FDA that 4 weight loss dietary supplements sold and marketed by the firm contain an undeclared drug ingredient. The FDA lab analyses of dietary supplements distributed by the company were found to contain undeclared Sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss. The FDA...
  • Propofol Injectable Emulsion 10 mg/mL 100 mL vials Recalled
    Teva Pharmaceuticals USA is initiating a recall of Propofol Injectable Emulsion 10 mg/mL 100 mL vials, lot numbers 31305429B and 31305430B. The product lots identified are being recalled due to the presence of elevated endotoxin levels in some vials within these lot numbers. Teva has been notified of 41 propofol-treated patients who experienced post-ope...
  • Illinois Firm Recalls Ground Beef Products Due To Possible E. coli O157:H7 Contamination
    E. S. Miller Packing Co., is recalling approximately 219 pounds of ground beef products that may be contaminated with E. coli O157:H7. The products subject to recall include: 10-pound Cryovaced bags of bulk "EDWARD S. MILLER PACKING CO., GROUND BEEF." Each bag bears the establishment number "EST. 34342" inside the USDA mark of inspection and case...
  • Suspected Tampering Prompts Recall of Hardcore Energize Bullet and New Whey Liquid Products
    FDA, Health Canada Issue Warnings The U.S. Food and Drug Administration is warning consumers not to buy or use Hardcore Energize Bullet or New Whey liquid products sold in test tube-like vials due to suspected product tampering. The products are being recalled. The suspected tampering involved a utility knife blade found in one vial of Hardcore...
  • Suspected Salmonella Contamination Prompts Popcorn Seasoning Recall
    Kroger is reportedly recalling 3 store brand popcorn seasonings because they may be contaminated with Salmonella. The 3 brands are: Kroger Popcorn Seasoning – Movie Theater Butter Flavored, in 2.82-ounce jars with a sell date of June 8, 2010, and UPC code 011110 72445 Kroger Popcorn Seasoning – White Cheddar Flavored, in 2.82-ounce jars wi...
  • Transvaginal Mesh Deaths Reported as Injuries?
    Nov-25-16 York, PA: “A good number of attorneys have reported transvaginal mesh adverse events to the FDA on behalf of their clients/patients, but over 23,000 reports are from physicians,” says Madris Tomes, founder of Device Events and former FDA Program Manager. “Physicians are not great at reporting— this is a HUGE number.” Du...
  • Mattel, Fisher-Price to Pay $2.3 Million For Lead Paint Violations
    Mattel, Fisher-Price to Pay $2.3 Million For Lead Paint Violations Mattel Inc., of El Segundo, CA, and its wholly owned subsidiary, Fisher-Price Inc., of East Aurora, N.Y. have agreed to pay a $2.3 million civil penalty for violating the federal lead paint ban. The penalty settlement, which has been provisionally accepted by the U.S. Consumer Prod...
  • Attorney: It's Mind Boggling Ammonium Nitrate Was Used in Airbags
    Nov-9-16 Houston, TX: A new Takata-related airbag lawsuit has been filed against Honda and Takata, alleging a motorist was seriously injured when her airbag exploded during a car crash. Attorney Mo Aziz—of Abraham, Watkins, Nichols, Sorrels, Agosto & Aziz—is part of the team that filed a lawsuit on behalf of Serena Martinez and has been involved...
  • SmartMonitor 2 Infant Apnea Monitor Recalled by Respironics, FDA
    Respironics and FDA have notified healthcare professionals of a Class I recall of SmartMonitor 2 Infant Apnea Monitor used for the continuous monitoring of respiration and heart rate of infant patients in the home or in the hospital. The monitors may fail to sound an alarm during periods of temporary interruption of breathing or low heart rates. ...
  • HP Recalls Notebook Computer Batteries Due to Fire Hazard
    The U.S. Consumer Product Safety Commission (CPSC) and Health Canada, in cooperation with Hewlett-Packard (HP) Co., of Palo Alto, CA, today announced a recall of about 70,000 Lithium-Ion batteries used in HP and Compaq notebook computers. They are being recalled because the batteries can overheat, posing a fire and burn hazard to consumers. To date, HP...
  • Pasta & Co Issues Recall due to Possible Salmonella Contamination
    Pasta & Co of Seattle, WA, is recalling their Chinese Vermicelli Salad and Pot Sticker Salad, because it has the potential to be contaminated with Salmonella. The products were manufactured using chili oil recalled by Union International Food Co., and may be contaminated with Salmonella. Salmonella is an organism which can cause serious and somet...
  • Nationwide Recall of Lion Pavillion Hot-Pot Seasoning
    Lion Pavilion, Ltd., based in Brooklyn, NY, is recalling approximately 16,213 pounds of seasoning products, which contain cattle by-products that were ineligible for import to the U.S. The firm is recalling these products because China is not eligible to export beef products to the United States. The products subject to recall include:14-ounce pac...
  • Oaxaca Soft Mexican-Style Cheese Recalled due to Possible Listeria Contamination
    Torres Hillsdale Country Cheese is recalling Oaxaca soft Mexican-style cheese due to potential Listeria monocytogenes Listeria. The recalled Oaxaca cheese product was distributed to retails stores and delis in Illinois and Minnesota, in 10 pound balls, labeled with the name "Torres Hillsdale Country Cheese LLC" The recall encompasses production...
  • Dietary Supplements Recalled Nationwide due to Undeclared Drug Ingredient
    Universal ABC Beauty Supply has issued a nationwide recall of dietary supplement products found to contain the undeclared drug ingredient Sibutramine. Sibutramine is an FDA-approved drug used as an appetite suppressant for weight loss. The dietary supplements listed below are not supposed to contain Sibutramine. The FDA has not approved these products,...
  • Specialized 2009 Model Bicycles Recalled due to Risk of Serious Injury
    About 14,000 Specialized 2009 model bicycles are being recalled because the handlebars can break, posing a fall hazard to the rider. So far, Specialized has received 2 reports of the handlebar breaking during use, 1 of which caused a rider to suffer head trauma which resulted in unconsciousness and a puncture wound to the arm. This recall involves...
  • Reports of Serious Injuries Prompt Recall of 2004 Roubaix Bicycles
    About 3,000 2004 Roubaix Comp Roubaix Pro bicycles are being recalled because the cable stop on the bicycle can loosen, which can cause the rider to lose control and fall from the bike. To date, Specialized Bicycle Components Inc., the importer of the bikes, has received 2 reports of falls that resulted in fractures requiring medical attention and surge...
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