LAWSUITS NEWS & LEGAL INFORMATION
Search Results for
Sort by date 828 pages found matching toyota recalls- Zimmer-Biomet Shoulder: Buyer (Patient and Surgeon) Beware
May-25-17 Minneapolis, MN: Shoulder replacement surgery is a well-established and should be a straightforward procedure, unless your orthopedic surgeon is implanting a Zimmer Biomet shoulder that has failed and you are unfortunate to have one or two of the 3,600 implants that have been recalled. According to the University of Minnesota, improvements in surgi... - Catheter Injury Lawsuits following Catheter Recalls
May-20-17 Dallas, TX: In the wake of more than four million catheter recalls over the past year by numerous medical device manufacturers, dozens of patients have reported injuries and two wrongful death lawsuits have been filed due to broken catheters. In most of these injuries the catheter tips have fractured or other parts of the device have separated withi... - Class 1 Recall of Medtronic SC Catheters and Revision Kit Models
The Food and Drug Administration (FDA) has issued a notification to healthcare professionals of the Class 1 recall of Medtronic SC Catheters and Revision Kit Models: 8709SC, 8731SC, 8578, and 8596SC when paired with the Medtronic IsoMed Pump Model 8472, due to a design incompatibility resulting in a physical interference between the SC catheter connector and... - Spinach Recalled Due to Possible Salmonella Contamination
Ippolito International, LP of Salinas, California is voluntarily recalling 1,715 cartons of bunched spinach, because it has the potential to be contaminated with Salmonella. The voluntary recall comes after routine random testing of bunched spinach in Michigan by the USDA Microbial Data Program, collected and analyzed by the Michigan Department of Agri... - Class 1 Recall of LIFEPAK CR Plus Automated External Defibrillators
The FDA has notified healthcare professionals of a Class I recall of certain LIFEPAK CR Plus Automated External Defibrillators (AED) manufactured and distributed from July 9, 2008 through August 19, 2008. An extremely humid environment may cause the affected devices to improperly analyze the heart rhythm and may cause the device to delay or fail to del... - California Firm Recalls Beef and Bean Burritos for Possible Listeria Contamination
Windsor Foods is recalling approximately 2,268 pounds of beef and bean burrito products that may be contaminated with Listeria monocytogenes. The following products are subject to recall: 18-pound bulk cases containing individually wrapped "BUTCHER BOY RED CHILE BEEF & BEAN BURRITOS." Each case of Butcher Boy brand burritos subject to recall... - Class 1 Recall Issued for Penumbra Neuron 5F Select Catheter
Penumbra and FDA notified healthcare professionals of the Class 1 recall of the Neuron 5F Select Catheter, used to remove blood clots or foreign objects from blood vessels. Due to a manufacturing error, the catheters may contain pin holes and exposed wire braids which may result in a brain clot or a blood vessel puncture, and this may lead to possible d... - Canned Soup Recalled
A Class I recall has been issued for approximately 6,490 pounds of a chunky grilled steak with vegetables canned soup made by Bay Valley Foods, because the soup may be underprocessed. The following product is subject to recall: 18.6 - oz. metal cans of Stater Bros. brand, "CHUNKY GRILLED SIRLOIN STEAK WITH VEGETABLES" Ready to Serve Soup. The front... - Airbag in Salvaged Used Car Explodes in Minor Crash
May-1-17 Las Vegas, NV: A Nevada woman suffered serious injuries when the airbag in a used car that her father gave her as a gift exploded. "Karina Dorado’s trachea was punctured by shrapnel from an inflator in an otherwise minor crash in Las Vegas on March 3," according to the Las Vegas Review-Journal . "She was rushed to a trauma center, where surg... - Airbag Lawsuits Dismissed as Parties Try to Work Out Settlement
Apr-17-17 Winston-Salem, NC: Two lawsuits filed in North Carolina last year against Takata Corp. over defective airbag injuries were voluntarily dismissed in January 2017 in favor of trying to work out a settlement, according to the Winston-Salem Journal . The Winston-Salem Journal article did not disclose settlement details. The lawsuits, one filed in... - Stand 'n Seal Spray Respiratory Damage and Death
Washington, DC: It took two recalls, two deaths and at least 80 serious injuries to take the grout sealant Stand 'n Seal Spray , out of the marketplace. Most troubling is that the manufacturer knewÓ-for more than 18 monthsÓthat this dangerous product caused respiratory injuries. Roanoke Companies (now called BRTT) introduced the produ... - Frigidaire Recalls Washing Machines
About 35,000 Crosley®, Frigidaire®, Kelvinator®, Kenmore®, Wascomat®, and White-Westinghouse® clothes washers are being recalled by the importer, Frigidaire, because an internal defect in the washer's drain pump can cause heat to build up, posing a fire hazard to the consumer. This recall involves the Crosley®, Frigidaire®, Kelvinator®, Ken... - STEAM Dietary Supplements Recalled Nationwide
Nutracoastal Trading LLC announced today that it is conducting a voluntary nationwide recall of the company's dietary supplement product sold under the following name: STEAM. The Company has been informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA for Lot 80214 found that the product contains sulfoaildenafil, a... - Haifa Smoked Fish Recall
Haifa Smoked Fish, Inc is voluntarily recalling all Haifa Smoked Fish brand Cold Smoked Whitefish sold between December 7, 2008 and June 18, 2009. The product is being recalled because it has the potential to be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in you... - 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...