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.
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.
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.
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.
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.
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 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 CommentsCompanyThis 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 Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026) SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026) Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 (Posted: 5 days ago)A federal judge has selected an Enfamil lawsuit to serve as the first NEC infant formula bellwether trial, which is set to begin in July.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITLawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms (05/08/2026)Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil (04/24/2026)Similac NEC Lawsuit Payout Increased by $17M in Punitive Damages (04/14/2026)
Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024
Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)
SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026)
Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 (Posted: 5 days ago)A federal judge has selected an Enfamil lawsuit to serve as the first NEC infant formula bellwether trial, which is set to begin in July.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITLawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms (05/08/2026)Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil (04/24/2026)Similac NEC Lawsuit Payout Increased by $17M in Punitive Damages (04/14/2026)