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.
Smith & Nephew Knee Lawsuit Filed Over Problems After Replacement Surgery December 8, 2011 Staff Writers Add Your CommentsA product liability lawsuit has been filed against Smith & Nephew over allegedly defective knee implant components that failed less than two years after being implanted in a West Virginia man.ย The Smith & Nephew knee lawsuit was filed by Robert Morris and his wife, Jenny, in Kanawha Circuit Court in West Virginia.According to the complaint, Morris had a Smith & Nephew Journey knee replacement system implanted in January 2009, including a Journey Deuce Oxinium femoral component, a Journey Uni right medial tibial baseplate, a Journey Uni right medial tibial insert and a Genesis II resurfacing patellar component.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 COMPENSATIONIn April 2010, less than 15 months after surgery, the artificial knee failed, causing Morris to undergo revision surgery to have the components replaced.Morris is seeking compensatory and punitive damages, accusing Smith & Nephew of manufacturing and distributing defective knee components and failing to warn consumers about the risk of failure.The case is one of a growing number of Smith & Nephew Journey knee replacement lawsuits filed by consumers who have experienced similar problems with the system.In recent years, a number of Smith & Nephew recalls have been issued for different components involved in the knee replacement system.Nearly 40,000 Journey Uni Tibial Baseplates were recalled in early 2010, due to a number of reported failures, which suggested that the component may have a tendency to fracture or break. This could result in severe pain and instability, often resulting in the need for surgery to revise the Smith & Nephew knee replacement or replace the base plate.In February 2011, a study was presented to the American Academy of Orthopaedic Surgeons that found that 16% of Smith & Nephew Journey-Deuce knee implants began to fail within 21 months and 39% of recipients reported poor results after receiving the implant. Tags: Knee Replacement, Product Liability, Smith & Nephew Image Credit: |More Lawsuit Stories Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026 Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges September 10, 2026 LG Electric Range Lawsuit Alleges Defective Controls Caused House Fire September 10, 2026 3 Comments BETTY January 15, 2016 MY KNEE WAS DONE DEC, 2015.HAVE SEVERE PAIN ,SWELLING AND INSTABILITY. GOING TO THE DR. AT THE PRESENT.DONT KNOW THE FUTURE nowa January 8, 2016 My knee replacement has been such pain.Got have another surgery help fix my knee replacement.So much pain i can’t enjoy my days or nights. Verron April 6, 2012 I received a knee replacement at VA Hosp in Houston March, 2008. I began experiencing pain last year, when I had to walk through mud. The backward motion caused a sever burning that has been prevalent since, and the VA doctor in Des Moines stated he would have to replace all the components, hopefully which would relieve the pain. Any suggestions? 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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 Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026) Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)