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  • Boston Scientific: Oops, They Did It Again
    May-8-07 Los Angeles, CA: "Oops I did it again" is the name of a song by pop star Britney Spears. It could also be the motto of medical device manufacturers Guidant (now part of Boston Scientific) who recently issued yet another recall for defective defibrillators/pacemakers. The latest recall was announced April 5, 2007, and concerns some 73,000 Implantable...
  • Boston Scientific and Guidant Off to Texas Slaughterhouse
    Sep-6-06 Corpus Christi, TX The first, but by no means the last, Guidant trial is scheduled to begin on September 18, 2006, in Neuces County District Court in Corpus Christi, Texas before Judge Jack Hunter. The two plaintiffs, Louis Motal, 63, and Bernice Hinojosa, 65, are surviving patients implanted with Guidant's Ventak Prizm 2 defibrillators in 2001. The law...
  • Defective Autos make for Countless Personal Injuries
    Feb-19-08 Hunter Valley, CA Art Masaoka refers to himself as a professional consumer, particularly when it comes to vehicles. Masoaka is also an expert witness for trial purposes on lemon-law cases; he wants to share with other consumers his knowledge of, and experience with, defective automobile products , particularly safety concerns that can lead to personal...
  • Lethal Defects Of Bjork-Shiley Heart Valve
    Apr-24-06 An estimated 25 million Americans have one kind of medical implant or another. However an analysis of implant recalls over 10 years show that the average number of recalls per year was 40 and by 2001, the number rose to 117. The FDA regulates the implant industry, but many products reach the market with insufficient clinical testing, followed by very litt...
  • Mirapex - Two Victims - Same Horror Story
    Feb-16-06 In mid-2001, Joe Neglia went on a cruise to Alaska and that trip marked the beginning of his downward spiral into hell. The ship had a gambling casino on board and according to Joe, he was "instantly and savagely hooked on the slots." A major problem arose when he came back ashore. "When I returned from the cruise I began hitting the local casinos," he re...
  • SJS - Called A Fate Worse Than Death
    Jan-29-06 Until Susie Orme developed Stevens Johnson Syndrome, it was a condition she read about in medical textbooks and a difficult topic to study for on her postgraduate exams. Susie is a doctor and as such, she was able to diagnose her own SJS. However, "no amount of training could prepare me for the pain ahead," she said. Susie's SJS was a reaction to the a...
  • Mega Brands Reaches Preliminary Settlement over Magnetix Toys
    New York, NY: A defective product class action lawsuit filed against Mega Brands has reached a preliminary settlement this week, with the toymaker stating that, under the terms of the settlement, it will provide refunds for qualified US claimants. If approved, the settlement would refund the price of the magnet toys, which were recalled in 2006,...
  • U-Prosta Natural Products Recalled Nationwide
    Ottawa, ON : "U-Prosta Natural support for prostate health" is being recalled in Canada by Sunnylife International Inc. after the U.S. Food and Drug Administration (FDA) found the product contains undeclared terazosin hydrochloride, which is a prescription drug used to treat high blood pressure and enlargement of the prostate gland, and could cause seri...
  • Ocean Technology Systems Recalls Guardian Full-Face Diving Masks
    Washington, DC: Undersea Systems International Inc doing business as Ocean Technology Systems, of Santa Ana, CA, is recalling about 1,700 Guardian full-face diving masks sold in the US and a further 80 sold in Canada because the purge assembly on the diving mask can disengage from the regulator, resulting in loss of air to the diver. This poses a drow...
  • Nationwide Recall of All Lots of Povidine Iodine Prep Pads
    Washington, DC: H&P industries has initiated a voluntary product recall of ALL LOTS of POVIDINE PREP PADS manufactured by H&P Industries but which are private labeled for many accounts. This recall has been initiated due to results of the FDA' ongoing investigation and sampling efforts, and H&P Industries, Inc. internal investigation. The Pov...
  • Nationwide Recall of Concentrated Sodium Chloride Injection
    Washington, DC: A voluntary nationwide recall was initiated on March 15, 2011 to the User Level, is for Concentrated Sodium Chloride Injection, USP 23.4%, 30 mL Single Dose Vials and 100mL Pharmacy Bulk Packages. The recall was initiated because some of the vials of these lots may contain visible particulates. Potential adverse events after intr...
  • Vitalabs Recalls Whey Protein due to Salmonella Contamination
    Washington, DC: Vitalabs, Inc, Jonesboro, GA is recalling four specific lot numbers of Whey-26 Protein Powder due to concerns over potential Salmonella contamination. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy pe...
  • ACCU-CHEK FlexLink Plus infusion sets Recalled
    Washington, DC: Roche Insulin Delivery Systems announced today that it is notifying its customers and healthcare professionals about the recall of the ACCU-CHEK FlexLink Plus infusion set, because of the potential for under delivery of insulin due to a kinked/bent cannula when inserting the ACCU-CHEK FlexLink Plus infusion set. If this remains unnotice...
  • Shishamo Roe Capelin 4L Recalled Due To Potential Of C. Botulinum
    Washington, DC: Pacific American Fish Co, Inc. of Vernon, California is recalling SHI306 Shishamo 4L 5PC (23-28G) Wild, Pack 4/20TR, Lots 202885-2 & 201011-3, Master Carton information. Based on FDA Import Alert, this type of processing and size of product has the potential to be contaminated with Clostridium botulinum, a bacterium which can cause fo...
  • Biotab Recalls Extenze Nutritional Supplements
    Washington, DC: Biotab Nutraceuticals, Inc. ("Biotab") is conducting a voluntary recall of two lots of EXTENZE nutritional supplement tablets. Some packages bearing lot numbers 0709241 and 0509075 are counterfeit products containing undeclared drug ingredients that can pose a serious risk to health. Biotab learned about the problem after being no...
  • Walt Disney Recalls Children's Watches
    Washington, DC: Walt Disney Parks and Resorts, of Lake Buena Vista, FL, is recalling about 1,200 children's light-up watches because the watch battery current interacting with nickel in the watch's stainless steel back can cause skin irritation and/or burning sensations to children who are allergic to nickel. This recall involves Buzz Lightyear,...
  • Smoked Salmon Recalled
    Washington, DC: St James Smokehouse Inc, is recalling its Scotch Reserve Whiskey & Honey Smoked Scottish Salmon 4oz retails packs under Lot code:5797 & batch code: 4759 with UPC# 853729001151 due to potential contamination with Listeria Monocytogenes. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infecti...
  • Lead-Tainted Toxic Waste Brand Nuclear Sludge Candy Recalled
    Washington, DC: Circle City Marketing and Distributing, doing business as Candy Dynamics, Indianapolis, IN, is issuing a recall of all Toxic Waste® brand Nuclear Sludge® products, all flavors, 0.3 oz (8 g) size pieces. The product is imported from Pakistan. Testing by the company indicates that some products contain elevated levels of lead...
  • State Garden Salad Mixes Recalled
    Chelsea, MA: State Garden is conducting a recall of all Salad products produced in their plant on January 4, 2011 which correspond to trace back codes 45693 and 45703 due to a risk of contamination with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or e...
  • Rosebud Drop-Side Cribs Recalled due to Entrapment and Suffocation
    Washington, DC: The Land of Nod, of Northbrook, Il, is recalling about 300 Rosebud drop-side cribs because the drop-side rail hardware on the cribs can break or fail, allowing the drop side to detach from the crib. When the drop side detaches, a hazardous gap is created between the drop-side rail and the crib mattress in which infants and toddlers can...
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