Scope Infection Lawsuit Patients across the United States have filed medical scope infection lawsuits after contaminated endoscopes and duodenoscopes allegedly transmitted dangerous bacterial infections during procedures such as ERCP, colonoscopy, and other endoscopic treatments.
Spinal Cord Stimulator Lawsuit Spinal cord stimulator lawsuits allege that implanted pain devices malfunctioned, migrated, or caused nerve damage, often forcing patients to undergo revision or removal surgery.
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.
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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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
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.
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.
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.
Breast Mesh Lawsuit Lawyers are investigating breast mesh lawsuits for women who suffered infections, pain, or implant failure from internal bra implants used in breast reconstruction surgery.
DePuy ASR Hip Settlement Requires Registration by Jan. 6 January 2, 2014 Irvin Jackson Add Your CommentsIndividuals who have previously experienced problems with a DePuy ASR hip replacement, which resulted in the need for revision surgery, must register by January 6 to be part of the settlement program announced in November.Johnson & Johnson’s DePuy Orthopaedics division currently faces about 12,000 hip replacement lawsuits filed in state and federal courts throughout the United States following the recall of the DePuy ASR XL Acetabular Hip Systemย in 2010.The metal-on-metal hip replacement system was removed from the market after data suggested that about one out of every eight would fail within five years. However, more recent data has suggested that theย DePuy hip failure rateย may ultimately be substantially higher, likely ending up in the 35% to 45% range.Stay Up-to-Date Abouthip replacement lawsuitsAboutLawsuits.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 fieldsEmail* SIGN ME UPΔ Learn MoreStay Up-to-Date AboutHip Replacement LawsuitsAboutLawsuits.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 fieldsEmail* SIGN ME UPΔ Learn MoreAll of the complaints involve similar allegations that DePuy designed and sold a defective and unreasonably dangerous hip implant. The metal-on-metal design causes the release of metallic debris into the body as the metal parts rub against each other during normal wear and tear, according to claims presented by individuals who experienced catastrophic failure of their implant.In November, a DePuy ASR settlement program was announced, which will result in the manufacturer paying at least $2.4 billion to resolve claims, but the total benefits that may be available under the offer may reach as high as $4 billion after accounting for medical expense reimbursements and other costs.Under terms of the agreement, individuals who underwent hip revision surgery prior to August 31, 2013 due to problems with a DePuy ASR hip may be eligible to pursue compensation through the program that will provide an average of about $250,000 per claim, with additional damages available for “extraordinary” injuries. However, a registration deadline of January 6, 2014 is rapidly approaching for individuals who wish to participate.ASR Hip Settlement EligibilityAccording to a program overview (PDF), potential participants in the settlement must meet the following requirements:They must be a U.S. Citizen or legal resident of the United States.They had to have either the ASR XL Acetabular Hip System or the ASR Hip Resurfacing System implanted in a hospital in the United States or at a U.S. military hospital.They had to have had the ASR in place for at least 180 days.They had to undergo revision surgery to remove the ASR hip implant for reasons related to its recall on or before August 31, 2013.The amount that will be awarded is determined by a number of factors. A base award of $250,000 per claim will be provided, but that may be reduced by factors such as the length of time the implant was in place, whether the individual smoked at the time they underwent revision surgery, whether the same hip had undergone previous replacement surgeries before the ASR hip was implanted, whether they were obese at the time the artificial hip was implanted, their age at the time the hip was implanted, and whether patients who died after revision surgery had a cause of death due to problems unrelated to the ASR hip implants.For individuals who suffered โextraordinary injuriesโ, including complications associated with the revision surgery, additional compensation may be obtained from another pool of $475 million.The settlement program is not mandatory, and each individual will still have the option to decide whether to accept or reject the offer provided under the program. However, Johnson & Johnson has required that at least 94% of eligible claimants to accept the terms for it to proceed.While the hip replacement settlement is expected to resolve the majority of claims, it will not end the entire DePuy ASR litigation. Individuals who decline the offer and those who have not had to have their DePuy ASR hip replaced prior to August 2013 will still continue to litigate their claims. In addition, individuals who have their hips fail in the future will be able to seek compensation through new lawsuits.Prior to the settlement agreement being reached, only two DePuy ASR cases made it to trial nationwide, with aย California jury awarding $8.3 million in damagesย earlier this year and a second trial inย Illinois state court resulting in a defense verdictย weeks later.Additional bellwether trials were expected to begin early next year in the federal court system and New Jersey state court. However those cases will not go forward in light of this agreement. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin 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. Tags: DePuy ASR, Depuy ASR Hip, Hip Replacement System, Johnson & Johnson, Metal-on-Metal Hip Image Credit: |More DePuy ASR Hip Lawsuit Stories Hip Replacement Lawsuit Claims System Failure Caused Woman To Suffer โDusky Metal Diseaseโ June 5, 2026 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 0 CommentsPhoneThis field is for validation purposes and should be left unchanged.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 NoPost Comment I authorize the above comments be posted on this pageWeekly 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 TermΔ MORE TOP STORIES Parietene Hernia Mesh Lawsuit Alleges Defective Covidien Implant Caused Severe Nerve Damage, Chronic Pain (Posted: 2 days ago)Covidien faces a hernia mesh lawsuit from a man who says he suffered nerve damage and other injuries after the product failed, requiring removal surgery.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralex Hernia Mesh Failure Lawsuit Alleges Implant Design Led to Infection (10/15/2026)Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial (10/06/2026)Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 (09/11/2026) DraftKings Lawsuit Seeks Discovery Into Gambling Algorithms, Bonuses and VIP Rewards (Posted: 3 days ago)Attorneys for an Illinois man and the sportsbook DraftKings have filed a status report indicating the plaintiff wants the company’s algorithm data, while the sports betting app wants the case dismissed.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings AI Lawsuit Alleges Gambling Promotions Targeted Users Likely to Lose Money (10/07/2026)DraftKings ‘Free Bet’ Promos Targeted Problem Gamblers Using AI: Report (09/29/2026)Online Gambling Addiction Lawsuit Alleges DraftKings App Fueled Compulsive Sports Betting (09/25/2026) Boston Scientific Spectra WaveWriter Lawsuit Alleges Lead Fracture, Migration and Painful Electric Shocks (Posted: 4 days ago)A woman’s Boston Scientific Spectra WaveWriter SCS lawsuit claims improper hermetic seals lead to short circuits, failures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (10/16/2026)Master Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)
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