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.
Metal-on-Metal Hip Failures Often Happen In First Two Years: Study July 18, 2012 Austin Kirk Add Your CommentsMore than three-quarters of all failures involving metal-on-metal hip replacement systems occur within two years after surgery, according to the findings of a new study.ย Metal-on-metal hip replacements are a controversial design, which gained popularity over the past decade, before concerns emerged about an increased risk of failure and other problems caused by the microscopic metal particles that are released as the metal parts of the implant rub against each other.In this month’s issue of the medical journal Orthopedics, U.S. researchers found that most metal-on-metal hip implant failures occur within a few years after being implanted, although such devices are designed to last 15 to 20 years. The failures are usually caused by aseptic acetabular loosening, often requiring revision surgery, according to the findings.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 COMPENSATIONResearchers conducted a review of 80 patients who underwent revision surgery to removed failed metal-on-metal artificial hips. They found that 78% of those patients had the revisions within two years of getting the implant, and 98% had the metal hips removed within the first three years. Metal-on-metal hip replacement systems are supposed to last much longer.The investigation also revealed that 13% of those who needed revision surgery suffered from localized soft tissue reactions, which most experts believe is caused by the metal debris generated by the parts rubbing together, a condition known as metallosis.Concerns About Metal-on-Metal Hips FailingThe study adds to the body of evidence that has raised significant concerns regarding metal-on-metal hip replacement systems. Last month, an FDA advisory committee convened to discuss the safety issues surrounding the implants and advised that anyone who has an all-metal artificial hip get it X-rayed annually to check for problems. Those suffering pain and discomfort should also have a blood test to look for signs of chromium and cobalt ions, key indicators of metallosis.The advisory committee members also noted that there appeared to be almost no reason to use metal-on-metal hip implants.Sales of metal-on-metal hip replacements have fallen sharply over the past two years, and more research has been focused on the impact of these microscopic particles entering the blood stream since a recall was issued for DePuy ASR hip implants in August 2010.The Johnson & Johnson subsidiary Depuy Orthopedics issued an ASR hip recall after acknowledging that 12% to 13% of the implants were found to fail within the first five years. Since that time, thousands of DePuy ASR hip lawsuits have been filed against the manufacturer alleging that they failed to adequately research the design or warn about the risk of failures.Similar product liability lawsuits have also been filed over other metal-on-metal implants, including the DePuy Pinnacle hip, Biomet M2A-Magnum hip and Wright Conserve hip.Metal Concerns From Modular Hip ReplacementsIn addition to concerns surrounding metal-on-metal hip replacements, which feature a metal ball that rotates within a metal cup, recently similar problems have surfaced with the release of metallic debris among modular hip components, which feature a metal neck that fits within a metal stem to allow the surgeon to adjust the length of the femoral component to fit the patient.Earlier this month, a Stryker Rejuvenate hip recall was issued after it was discovered that the metal contact between the two components of the modular neck stems used in the system was associated with an increased risk of fretting and corrosion, which has been found to result in pain, swelling, local tissue reactions and early failure of the hip replacement.A number of lawsuits over failed Stryker modular hip replacmements are also now being reviewed by attorneys throughout the United States, and serious questions remain about the safety of any implants that feature direct metal-on-metal contact that bears the weight of the body during normal daily movements. Tags: Biomet M2A Magnum, Depuy ASR Hip, DePuy Pinnacle, DePuy Pinnacle Hip, Hip Replacement, Metal Hip Replacement, Metal-on-Metal Hip, Metal-on-Metal Hip Replacement, Metallosis, Wright Conserve Hip Implant Image Credit: |More Lawsuit Stories Lawsuit Claims Amazon Sold Kids Sunscreen With โAlarmingly Highโ Levels of Lead, Other Metals May 20, 2026 Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit May 19, 2026 Cartiva Toe Implant Erosion Resulted in Persistent Pain, Lawsuit Alleges May 19, 2026 0 Comments URLThis 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 Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: yesterday)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro 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) Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: 2 days ago)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: 5 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)
Lawsuit Claims Amazon Sold Kids Sunscreen With โAlarmingly Highโ Levels of Lead, Other Metals May 20, 2026
Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: yesterday)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro 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)
Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: 2 days ago)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: 5 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)