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  • FDA, Thomas Medical Issue Class 1 Recall of Coronary Sinus Guide Systems
    Washington, DC: The FDA and Thomas Medical Products Inc, notified healthcare professionals of a Class I Recall of certain lots of the product, tube-like devices placed into blood vessels to insert pacing or defibrillator wires and catheters into blood vessels. The sheath tip may break off and separate while the sheath is inside a blood vessel. If...
  • FDA Issues Recall on Medtronic Implantable Pain Pumps
    Mar-17-17 Silver Spring, MD: Six months after Medtronic issued a voluntary recall on certain potentially defective catheters , the Federal Drug Administration has announced an update on a previous recall on two of Medtronic's implantable drug pumps. The FDA on March 14 announced a recall on Medtronic's SynchroMed II and SynchroMed EL implantable drug infusion...
  • The FDA Shortcut to a Hip Replacement Lawsuit
    Feb-22-17 Bergen, NJ: It was back in 2008 that Hip Replacement Implant Failure caught up with Zimmer, when its Alumina Ceramic Femoral Head component was subject to a Class 2 recall by the US Food and Drug Administration (FDA). According to the official recall posting , Zimmer stated the reason for the recall: “When used with cobalt/chromium hip stems,...
  • INRatio Class Action Headed for Trial
    Feb-7-17 Los Angeles, CA The Alere INRatio home monitoring system offered warfarin (Coumadin) users a convenient way to test their blood clotting rate without having to go the doctor’s office or a laboratory. Instead, they got an expensive, unreliable and potentially dangerous product. They want their money back. Thousands of people who purchased...
  • Despite $1B Penalty by the Feds, It’s Not Over Yet for Takata: Airbag Injuries
    Feb-1-17 Washington, DC: The massive $1 Billion criminal penalty announced by the US Department of Justice earlier this month surrounding defective Takata airbags is not, in reality, an end to the troubles for the beleaguered Japanese manufacturer. Just one day after the Christmas holiday this past December, German automotive manufacturer BMW announced a recall of...
  • Nationwide Recall of All Accusure Insulin Syringes
    Qualitest Pharmaceuticals today issued a voluntary nationwide recall of all Accusure Insulin Syringes. The distributed syringes are of the following descriptions and NDC numbers: 28G 1/2cc, NDC 0603-6995-21;28G 1cc, NDC 0603-6996-21; 29G 1/2cc NDC 0603-6997-21, 29G 1cc, NDC 0603-6998-21, 30G 1/2cc, NDC 0603-999-21, 30G 1cc, NDC 0603-7000-21, 31G 1/2cc,...
  • Adverse Events for Patients Using Alere INRatio System
    Jan-21-17 Houston, TX: Patients taking blood thinning medications know they have to be careful to ensure their blood remains in therapeutic levels, to prevent major bleeding episodes. That’s why they use devices like the Alere INRatio2 system, to ensure that if they need it, their blood clots properly. But what happens if they can't be sure the systems tha...
  • People Angry with Department of Motor Vehicles Violating their Privacy
    Jan-19-17 Charlotte, NC: “It’s reassuring that attorneys are trying to stop the DMV from selling our private information ,” says Gary. “I wondered how these companies got my address and phone number—until I read on LawyersandSettlements about an attorney filing complaints about DPPA violations.” Gary is referring to attor...
  • 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...
  • Surgical Mesh Lawsuit to Proceed
    Dec-23-16 Providence, RI: A Rhode Island man who received recalled abdominal mesh just prior to a product recall in 2005, will see his surgical mesh lawsuit go forward after a Rhode Island judge refused to dismiss the case. According to court documents Wayne Smith received the Composix Kugel Hernia patch abdominal mesh for repair of a ventral hernia. Not long...
  • 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...
  • Fire Department Sees Two Dehumidifier Fires in Sheboygan
    Dec-8-16 Sheboygan, WI Battalion Chief Gary Kolberg from the Sheyboygan Fire Department in Sheboygan, Wisconsin says the dehumidifier in the house his firefighters were called to was so incinerated he couldn’t even tell what the serial number was on the unit. “It was so destroyed it is impossible to say what happened to it and there was a lot of other mater...
  • 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...
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