Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
Hair Relaxer Lawsuit Regular exposure to chemicals in hair relaxer may cause uterine cancer, ovarian cancer and other injuries. Women diagnosed with cancer may be eligible for settlement benefits.
Depo-Provera Lawsuit Depo-Provera lawsuits are being investigated for women who developed meningioma brain tumors after receiving Depo-Provera birth control shots, claiming that Pfizer failed to adequately disclose side effects.
Nitrous Oxide Lawsuit Individuals who suffered harm, or families who lost a loved one after using nitrous oxide products may be eligible for financial compensation through a nitrous oxide lawsuit.
Sports Betting Addiction Lawsuit Sports betting addiction lawsuits are being investigated for college students and young adults who developed gambling problems after using apps like FanDuel and DraftKings, alleging that the platforms failed to warn about the addictive nature of their features and marketing practices.
Ozempic Lawsuit Lawyers are pursuing Ozempic lawsuits, Wegovy lawsuits and Mounjaro lawsuits over gastroparesis or stomach paralysis, which can leave users with long-term gastrointestinal side effects
Suboxone Tooth Decay Lawsuit Lawsuits are being pursued by users of Suboxone who experienced tooth loss, broken teeth or required dental extractions. Settlement benefits may be available.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
Bard PowerPort Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
AngioDynamics Port Catheter Lawsuit Serious and life-threatening injuries have been linked to problems with Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.
Problems with DePuy Metal-on-Metal Hips Continue to Rise: Doctors March 22, 2013 Irvin Jackson Add Your Comments Revision surgery rates for the recalled DePuy ASR hip replacement system are continuing to rise, according to a new report from an Illinois doctor. A study presented at annual meeting of the American Academy of Orthopaedic Surgeons this week indicates that one facility is still seeing an increasing percentage of patients who required revision surgery after experiencing problems with the DePuy metal-on-metal hip, which was pulled from the market three years ago amid concerns about an increased risk of premature failure. The report was presented by Dr. Chris J. Dangles of Carle Foundation Hospital, in Champaign, Illinois. At his facility, nearly a quarter of all DePuy ASR hip implants have been replaced, and about half of all women who received one of the recalled hips have had revision surgery. The 24% revision surgery rate came after only four years of use. Stay Up-to-Date About hip replacement lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments. "*" indicates required fields Email* SIGN ME UP Δ Learn More Stay Up-to-Date About Hip Replacement Lawsuits AboutLawsuits.com sends a weekly digest email with information about recalls, lawsuits and warnings that may impact your family, which will include any new hip replacement lawsuit updates or developments. "*" indicates required fields Email* SIGN ME UP Δ Learn More High Failure Rates Led to Recall, Lawsuits A DePuy ASR recall was announced in August 2010 after the manufacturer, DePuy Orthopaedics, a subsidiary of Johnson & Johnson, warned that the metal-on-metal hip replacement system appeared to suffer a 12% to 13% failure rate after five years. However, many independent experts have predicted that the DePuy ASR hip failure rate will actually be much higher, with some estimating that a third of all DePuy ASR metal-on-metal hips could fail after just six years. Carle Foundation Hospital quit using the implants 18 months before the recall, due to the high rate of complications seen by health care professionals there, Dangles reported. Johnson & Johnson faces thousands of product liability lawsuits over the DePuy ASR hip, which have been brought by patients who experienced problems from metal blood poisoning caused as the metal parts rub against each other, which often results in the need for revision surgery. Most of the DePuy ASR litigation is currently pending in the federal court system, where complaints filed in U.S. District Courts throughout the country have been consolidated as part of an MDL, or multidistrict litigation, before U.S. District Judge David Katz in the Northern District of Ohio. Trials Over DePuy Metal-on-Metal Hip Problems As of March 5, at least 7,235 lawsuits over the DePuy ASR hip were consolidated in the federal MDL, according to the latest update (PDF) by the U.S. Judicial Panel on Multidistrict Litigation. There are also a number of DePuy lawsuits pending in state courts throughout the country. Earlier this year, the first case in the country was presented to a California state court jury, which awarded $8.3 million in damages against Johnson & Johnson as a result of the DePuy ASR hip. Another trial is currently underway in Illinois state court, involving a lawsuit filed by a 54 year old nurse who alleges that she had to undergo revision surgery and has been left with substantial permanent injuries. In the federal court system, a small group of cases in the DePuy ASR MDL are being prepared for early trial dates, known as “bellwether” cases. The first federal DePuy ASR hip lawsuit is expected to go before a jury on May 6, involving a complaint filed by Faye Borney-Madgitz, with a second trial scheduled to begin on July 8, involving a complaint filed by Ann McCracken. In addition to lawsuits over the DePuy ASR implant, individuals have filed lawsuits over other metal-on-metal implants, including the Biomet M2A Magnum, the Wright Medical Conserve Cup, and the DePuy Pinnacle hip. Tags: DePuy, Depuy ASR Hip, Johnson & Johnson, Metal-on-Metal Hip Replacement, Metallosis Image Credit: | Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. More DePuy ASR Hip Lawsuit Stories Biomet Hip Lawsuit Filed Over Defective M2A Metal-on-Metal Implant December 26, 2024 Zimmer Biomet Lawsuit Filed Over RibFix Blu Implant Fracture September 25, 2024 Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024 0 Comments Share Your CommentsFirst Name*Last NameEmail* Shared Comments*This field is hidden when viewing the formI authorize the above comments be posted on this page Yes No Post Comment I authorize the above comments be posted on this page Weekly Digest Opt-In Yes, send me a weekly email with the latest lawsuits, recalls and warnings. Want your comments reviewed by a lawyer?To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.Contact Phone #Alt Phone #Private CommentsNOTE: Providing information for review by an attorney does not form an attorney-client relationship.CAPTCHAGA SourceGA CampaignGA MediumGA ContentGA TermCommentsThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Lawsuit Claims Cartiva Implant Caused Bone Loss and Nerve Damage in Big Toe (Posted: yesterday) A Cartiva implant lawsuit blames the manufacturer for failing to warn patients about high failure rates for years after it began receiving implant complication reports. 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