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.
Compensation for DePuy ASR Hip Implants Should Be Paid to All Patients, According to India Government September 11, 2018 Irvin Jackson Add Your CommentsThe government of India is ordering the makers of the DePuy ASR hip system to track down and pay compensation to all individuals who received the recalled metal-on-metal hip replacement in that country.A letter from India’s Ministry of Health & Family Welfare was sent to DePuy International U.K., a Johnson & Johnson subsidiary, following an August 30th order (PDF) by the Central Government to create a committee to determine the amount of compensation required for recipients of the recalled hip implants.Aย DePuy ASR recallย was issued in August 2010, after the manufacturer acknowledged that a higher-than-expected number of the metal-on-metal hip implants were failing within a few years after surgery. While original estimates suggested that about one out of every eight may fail within five years, subsequent data has indicated that the DePuy ASR failure rate may be substantially higher.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 MoreThe hip replacement design features a metal femoral head that rotates within a metal acetabular cup, resulting in the release of metallic debris as the metal-on-metal parts rub against each other during normal daily activities. This debris can cause metal blood poisoning, known has hip metallosis, with can lead to the loosening and ultimate failure of the artificial hip.In the U.S.ย Johnson & Johnsonโs DePuy Orthopaedicโs subsidiary agreed toย pay more than $3 billion to settle ASR cases in 2013.More than 12,000 DePuy ASR hip cases were filed prior to the original settlement, but it is estimated that 90,000 of the implants were sold world-wide before the design was recalled in August 2010.There were reportedly about 4,700 DePuy ASR hip procedures performed in India from 2004 through 2010. However, the ASR hip helpline in that country has only located 1,080 of those patients. As a result, rhe government is requiring DePuy to trace down the remaining patients and collect data on their health status and the status of the hip implant.It must then pay them adequate compensation, based on the level of their pain, disability, suffering, and loss of wages. The Indian government estimates the required Hipcompensation is about $28,000 per patient. 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, Hip Replacement System, Johnson & Johnson, Metal-on-Metal HipMore DePuy ASR Hip Lawsuit Stories Metal-on-Metal Hip Problems Known for Years by DePuy Orthopaedics: Report April 12, 2017 Verdict in DePuy Pinnacle Hip Lawsuit Reduced To $151M, But Additional Trials to Proceed July 11, 2016 DePuy Pinnacle Hip Failures and Revision Surgery Rates Unacceptably High: Study May 5, 2016 0 CommentsInstagramThis 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 SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: yesterday)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: 2 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) Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: 3 days ago)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
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