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.
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
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.
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.
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.
Metal-on-Metal Hip Lawsuit Filed Against Johnson & Johnson and DePuy November 17, 2010 Staff Writers Add Your CommentsA New York woman has filed a metal-on-metal hip replacement lawsuit against Johnson & Johnson and its subsidiary, DePuy Orthopaedics, alleging that a DePuy ASR hip implant she received was defective and failed, causing her to suffer painful and debilitating injuries.ย The lawsuit was filed earlier this month by Annie OโNeill, 67, of Gardiner, New York, in federal court in California. The complaint alleges that Johnson & Johnson and DePuy failed to warn patients about the risk of problems with metal-on-metal ASR hip replacements and failed to promptly issue a recall once it became clear that a large number of the implants were failing shortly after surgery.OโNeill received a DePuy ASR hip in May 2009, but the implant detached from her acetabulum over the following months and caused her severe pain and problems walking. Eventually, the implant began emitting noise from her hip when she walked, which continually grew louder. Between the pain and the noise from the defective implant, it was decided that OโNeill should undergo hip revision surgery on July 26, 2010.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAccording to the complaint, OโNeill is a nature enthusiast who enjoyed hiking and rock climbing, but even after surgery to fix the DePuy ASR implant problems she continues to have trouble walking.In August, a month after O’Neill’s hip revision surgery, Johnson & Johnson and DePuy recalled the ASR XL Acetabular Systems, saying that the metal-on-metal hip implant had a 13% failure rate. They also recalled the ASR Hip Resurfacing System, which had a 12% failure rate. About 93,000 of the artificial hip systems were sold prior to the recall.A growing number of individuals throughout the United States have filed a similar DePuy ASR metal hip lawsuit after they experienced problems from the defective implant. This week, the U.S. Judicial Panel on Multidistrict Litigation is scheduled to meet to determine whether the DePuy ASR hip replacement litigation should be consolidated in federal court for pretrial proceedings.All of the claims involve similar allegations of design defect, which caused the plaintiffs to incur additional medical expenses, suffer pain and, in some cases, require additional surgery to revise or replace the hip implant. The complaints allege that DePuy failed to adequately test the metal-on-metal hip system and failed to immediately issue a recall when it became apparent that that the DePuy ASR was linked to a high failure rate. Tags: California, DePuy ASR, Depuy ASR Hip, Hip Implant, Johnson & Johnson, Metal-on-Metal Hip, New York, Personal Injury Image Credit: |More Lawsuit Stories Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL July 31, 2026 Ocoopa Hand Warmer Recall Issued After 350 Burn Injuries, One Death July 31, 2026 Depo-Provera Settlement Information to Be Presented Through Town Hall Meeting July 30, 2026 2 Comments Monika February 9, 2013 I had revision surgery on Jan 7/13 after a long year of pain and suffering. I was walking with much difficulty, swaying from side to side and could only walk short distances ie. a few houses down the street. The original total hip replacement was done April 6 2009. I could not understand what was happening until I received notification from a lawyer. At that time I contacted my surgeon, although it should have been much sooner! I don’t recall having cobalt and chromium levels done but I did have xrays and ultrasound. I was then instructed to return in another six months, which I did. It was decided at that time that I needed the revision. I am now recuperating at home after discharge from a rehab. My walking is much improved although I still need to use my cane and be aware of all the precautions. I am not driving as yet. I look forward to having the ability to participate more in activities which require walking. I am registered with a lawyer at the present time and have not heard anything back as yet except for the fact that they have my Depuy ASR joint in a forensic lab for safekeeping. There is a class action lawsuit going on and I was told that a court date was set for Feb. 6. It is now Feb. 9 . I am relieved to have the surgery overwith, but also worry about the loss of wages in the meanwhile. I hope they get things settled quickly. Donald November 18, 2010 I had a hip replacement, metal on metal, DePuy KA11 stem, Pinnacle 100 acetabular cup etc and it is failing. My surgery was 12/1/09. My surgeon used the anterior approach. He has since left the practice. Now, the senior guy in the practice says I need a replacement, not metal on metal and he would use the posterior approach and cut muscle. Who is the best orthopedic guy in the country to fix this problem? FacebookThis 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 Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (Posted: today)Lawyers involved in Boston Scientific spinal cord stimulator lawsuits have proposed an organizational structure for those chosen to represent the needs of all plaintiffs in the litigation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)Boston Scientific Spinal Cord Stimulator Lawyers to Meet With MDL Judge for Initial Conference Aug. 5 (07/16/2026) Depo-Provera Settlement Information to Be Presented Through Town Hall Meeting (Posted: yesterday)A federal judge has reviewed a Depo-Provera settlement agreement that could resolve thousands of brain tumor lawsuits, indicating that details of the confidential plan will be revealed to plaintiffs at a future hearing.MORE ABOUT: DEPO-PROVERA LAWSUITNew Study Adds to Evidence Depo-Provera Injections Cause Meningioma Brain Tumor Risks (07/13/2026)Depo-Provera Lawsuit Settlement Agreement May Resolve Eligible Meningioma Claims in MDL (06/15/2026)Depo-Provera Meningioma Side Effects Left Woman With Debilitating Migraines, Lawsuit Claims (06/05/2026) J&J Agrees to $5.5B Talcum Powder Settlement Payout to Resolve Ovarian Cancer Lawsuits (Posted: 2 days ago)A $5.5 billion settlement deal could resolve nearly 80,000 talcum powder cancer lawsuits that claim Johnson & Johnson products were contaminated with asbestos.MORE ABOUT: TALCUM POWDER CANCER LAWSUITSAdditional Talks To Settle Talcum Powder Cancer Lawsuits Set for April 13 (03/20/2026)Ovarian Cancer Talcum Powder Lawsuit Results in $250K Verdict Against J&J (02/16/2026)Evidence That Baby Powder Causes Ovarian Cancer Should Be Admissible At Trial: Report (01/22/2026)
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