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Sort by date 828 pages found matching toyota recalls- FDA Issues Class 1 Recall of Zimmer M/L Taper with Kinectiv Technology Prosthesis
Washington, DC: The US Food and Drug Administration (FDA) and Zimmer have issued a Class 1 recall of the Zimmer M/L Taper with Kinectiv Technology Femoral Stems and Necks are Tivanium® alloy implants used for hip replacements. The company found a process monitoring failure that led to higher than expected amounts of manufacturing residues left... - Anti-Coagulation Medications Lawsuit News and Legal Information
Anti-coagulation lawsuits have been filed against the makers of certain anti-coagulation medications alleging the makers of those medications did not carry adequate warnings about the risks of anti-coagulation side effects . Side effects associated with certain blood thinners include an increased risk of life-threatening uncontrolled bleeding. Anti... - FDA Finally Pulls Zantac
Apr-17-20 Washington, DC Since at least last summer the FDA has known that a contaminant known as N-Nitrosodimethylamine (NDMA) was present in ranitidine medications (commonly known as the brand name Zantac ), but the agency didn’t order a withdrawal of the popular heartburn drug until this month – almost a year later. Chances are, countless people who... - Syngenta GMO Corn Seed Lawsuit Legal News and Information
Hundreds of Syngenta Genetically Modified Corn Seed Sales lawsuits have been filed nationwide, claiming Syngenta knew, or should have known, that its genetically modified Viptera corn seed (Agrisure Viptera or MIR 162) and Duracade corn seed would contaminate US corn shipments and prevent the corn from being sold to export markets, particularly Ch... - Zantac Cancer Lawsuits Move to MDL Phase
Mar-20-20 West Palm Beach, FL Zantac cancer lawsuits will be consolidated in multidistrict litigation in the U.S. District Court for the Southern District of Florida. At the time of its formation on February 6, the MDL included 15 cases. An additional 126 cases were pending in 21 districts nationwide, and more plaintiffs are expected to join. The consolidated la... - Tylenol/Acetaminophen Side Effects
Tylenol is one of the most popular painkillers in the world, yet it has been linked to a number of serious Tylenol side effects . Attorneys are investigating Tylenol overdose and Tylenol liver damage claims stemming from acetaminophen toxicity , and are subsequently filing Tylenol lawsuits . Tylenol Side Effects Tylenol overdose is no... - Does Bayer Regret Buying Monsanto?
Oct-18-19 St Louis, MO: About 18,400 Monsanto glyphosate lawsuits alleging Roundup cancer are bound to put a large dent into the $63 billion that Bayer bought St. Louis-based Monsanto for last year. While Bayer knew it inherited the Roundup lawsuits, one plaintiff attorney believes the German pharmaceutical company wasn’t anticipating the high cost of losing. ... - Defective Goodyear RV Tires
A popular Goodyear RV Tire has a serious design flaw and can potentially cause an accident resulting in serious injury or death. There have been reports of Goodyear Tire Model #G159 in size 275/70 22.5 failing without warning and causing serious accidents involving the RV they were mounted on. This model Goodyear tire has a history of de-treads and failure... - Hip & Knee Replacement Implant Failure - Hip Replacement Lawsuit & Lawyer
The past decade has seen an exponential increase in hip and knee replacements and with it, hip & knee replacement failure . With more and more baby boomers approaching an older age, hip and knee replacement surgery is becoming more common--as are hip and knee replacement complaints . Since the Depuy hip and knee replacement recalls in 2005, thousands... - Hip and Knee Replacement FAQ
Why are hip and knee implant devices being recalled? Some hip and knee implant devices are being recalled because of high failure rates that result in patients requiring revision surgery years before they typically should. For example, most hip implants are expected to last approximately 15 years, but with some implant devices, such as the DePuy ASR h... - US DOT: Your Car and Where You Live May Increase Defective Airbag Risk
May-25-18 Miami, FL: Of about 50 million Takata defective airbags being recalled, some vehicles are more dangerous than others, according to the US. Department of Transportation. And some places have a greater potential to cause inflator ruptures—heat and humidity are risk factors. For instance, if you live in Florida or Puerto Rico and drive a Ford Ranger or... - HP Expands Recall of Notebook Computer Batteries
Washington, DC: Hewlett-Packard Company is recalling lithium-ion batteries used in HP and Compaq notebook computers because the batteries can overheat and rupture, posing fire and burn hazards to consumers. About 162,600 batteries are affected by this recall, 54,000 and 70,000 batteries were previously recalled in May 2010 and May 2009, respectively... - Pentrexyl Forte Natural Recalled for Misleading Packaging
Washington, DC: Phoenix Import & Distribution LLC is recalling for PENTREXYL FORTE NATURAL because the packaging is believed to be misleading, causing it to be confused with an antibiotic. The product is packaged in a green and white box, containing 30 red and white capsules. PENTREXYL FORTE NATURAL is a Dietary Supplement only and does not contain ant... - J&J to Pay $10 Million in SJS Case
Washington, DC: A jury in Pennsylvania has ruled that Johnson & Johnson (J&J) must pay $10 million in damages to the family of a little girl who suffered adverse effects known as Stevens-Johnson Syndrome, after taking Children's Motrin. Brianna Maya took the Motrin to treat a fever and cough in 2000. She suffered skin burns and eye dama... - American Regent Issues Nationwide Recall of Sterile Water for Injection
Washington, DC: American Regent is conducting a nationwide voluntary recall to the consumer and user level of the following product: Sterile Water for Injection, USP, 50 mL Single Dose Vial, NDC # 0517-3050-25, Lot 0092, Exp. Date February, 2014 This recall, initiated on May 19, 2011 to the User or Consumer Level, is for Lot 0092 Only... - Boss Pet Recalls Pig Ear Products due to Possible Salmonella Contamination
Washington, DC: Boss Pet Products, Inc. announced that it is recalling its Diggers Natural Treat Pig Ear pet treats because the products have the potential to be contaminated with Salmonella. Boss Pet has been notified by one of its suppliers, Keys Manufacturing Company, Inc., that a batch of Keys' pig ear treats tested positive for Salmonella... - Multi-Mex Distributor Recalls Dietary Supplements following Pediatric Hospitalizations
Washington, DC: Multi-Mex Distributor, Inc has recalled dietary supplements that may be labeled as antibiotic drugs. The recall was initiated after an FDA inspection revealed the product packaging mimics antibiotics readily available in Mexico and possibly familiar to Hispanic consumers. The products were distributed in the following states: Geor... - Takata Settles with 44 States. No Dough, Though
Mar-1-18 Washington, DC Takata airbag failures have already killed 22 people and injured nearly 200 more. The ensuing lawsuits and recalls affect nearly 13 percent of registered vehicles in the United States (and as many as a third of the cars on the road in Australia). It was the largest automotive recall in history, and it drove the company into bankruptcy... - Fresh Express Recalls Bag Spinach Due to Possible Risk from Salmonella
Washington, DC: Fresh Express is recalling 2,939 cases of 9 oz. Bag Spinach with Product Codes starting with H081 and H082, UPC Code of 7127913204 and Use-by Dates of April 6 and 7 out of an abundance of caution due to a positive test result for Salmonella from random sample testing. The company is not aware of any illnesses reported in connection... - Citalopram and Finasteride Recalled
Washington, DC: Greenstone LLC is recalling, to the patient level, medicines with lot number FI0510058-A on the label. This includes Citalopram 10mg Tablets (100-count bottle) and Finasteride 5mg Tablets (90-count bottle), both distributed in the U.S. market. The recall is due to the possibility that incorrect labels have been placed on the b...