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 Two-to-Three Times Higher Than Other Implants January 20, 2014 Irvin Jackson Add Your CommentsAccording to recent information released by groups representing orthopedic surgeons, metal-on-metal hp replacements appear to be two-to-three times more likely to fail when compared to other types of artificial hip systems.In this month’s issue of the Journal of Bone and Joint Surgery, the American Association of Hip and Knee Surgeons, the American Academy of Orthopaedic Surgeons, and The Hip Society issued a consensus statement warning about the risk of problems with metal-on-metal hips, which have been linked to a number of recalls and lawsuits in recent years.“It has been estimated that since 1996 more than 1,000,000 MoM articular couples have been implanted worldwide,” according to the statement. “However, with increasing clinical experience, the national joint registries have recently reported the failure of total hip arthroplasty (THA) with MoM bearings to be two to threefold higher than contemporary THA with non-metal-on-metal bearings.”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 statement points out that in addition to actual catastrophic structural failures, adverse tissue reactions caused by metal debris shed by metal-on-metal hip implants is also being recognized as an important reason for the high failure rates.While the consensus paper acknowledges that each patient has individual needs and does not outright call for other orthopedic surgeons to never use metal-on-metal hip systems, the statement may be the final blow for metal-on-metal designs, which rose to prominence several years ago under the belief that they would be more durable and more appropriate for young, active artificial hip recipients.After the new hip design gained widespread use, a number of orthopedic surgeons began expressing concerns over the metal ball-and-socket hip designs when they started to see a high number of their patients return due to failures, tissue reactions and other problems. Surgeons noted that as the metal pieces rub against each other during normal use, cobalt and chromium debris may be shed into the body. This can lead to catastrophic failures and there were concerns that the debris was causing metallosis, a form of metal blood poisoning, and leading to the development of pseudotumors and dead tissue around the implants.The issue gained national attention in August 2010, following a recall of the Depuy ASR XL Acetabular hip replacement and resurfacing systems. DePuy Orthopaedics, a division of Johnson & Johnson, announced that the artificial hips had a failure rate of up to 13%. That number has been signficantly revised over the years, with some experts and analyses predicting about a third of the DePuy ASR hips will fail within six years.Following that recall and high failure rates involving other metal-on-metal hip implants, surgeons began to quickly back away from the use of the design, and this month’s consensus statement may result in many orthopedic surgeons swearing off metal-on-metal hip replacement systems entirely.Manufacturers continue to face thousands of metal-on-metal hip replacement lawsuits brought by individuals nationwide. While hip implants are typically expected to last 15 to 20 years, most of the plaintiffs allege that they experienced complications within a few years that result in the need for revision surgery.More than 12,000 DePuy ASR hip lawsuits have been filed against Johnson & Johnson, and the manufacturer is expected to pay more than $2.4 billion to resolve about 8,000 cases under a recently proposed settlement program.Similar lawsuits are pending against manufacturers of other metal-on-metal hip lawsuits, including theย DePuy Pinnacle,ย Biomet Magnum, and theย Wright Medical Conserve Cupย . 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: Biomet Magnum, DePuy ASR, DePuy Pinnacle, Johnson & Johnson, Metal-on-Metal Hip Replacement, Metallosis, Wright Conserve Hip Implant 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 1 Comments Howard May 12, 2015 Why are they still on the marketEmailThis 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 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: yesterday)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026) Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: 2 days ago)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026) WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 3 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)
Zimmer Biomet CPT Hip System Linked to Increased Risk of Thigh Bone Fractures, FDA Warns September 18, 2024
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: yesterday)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)
Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: 2 days ago)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)
WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 3 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)