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.
Lawsuit Over Recalled DePuy ASR Hips Filed by 13 from Illinois and Indiana October 7, 2010 Staff Writers Add Your CommentsA state court DePuy ASR hip lawsuit has been filed on behalf of 13 people from Illinois and Indiana who claim that they received a recalled metal-on-metal hip implant made by DePuy Orthopaedics that subsequently had to be replaced as a result of design defects.ย The lawsuit over the recalled DePuy ASR hips was filed last month in Champaign County Court in Illinois. It is one of a growing number of product liability lawsuits filed against DePuy and their parent company, Johnson & Johnson, in state and federal courts throughout the United States following a DePuy hip recall issued in August.Approximately 93,000 DePuy ASR XL Acetabular System implants and DePuy ASR Hip Resurfacing System implants were recalled after data suggested that about one out of every 8 people who received one of the devices may experience problems with their DePuy ASR hip within five years after implant, with many requiring risky hip revision surgery to replace the metal-on-metal artificial hip.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 COMPENSATIONWhile a handful of lawsuits over the hip implant were filed prior to the recall, the number of claims has increased dramatically as individuals return to their doctors for a re-evaluation and discover that they are experiencing complications from the DePuy metal hip. Although the recall does not mean that all implants must be replaced, doctors are encouraging all patients to return for an evaluation to determine whether the hip replacement is functioning as it is supposed to.The complaint filed in Illinois raises similar allegations to those found in other lawsuits over the DePuy ASR hip recall, indicating that the manufacturer failed to adequately test the metal-on-metal hip system and failed to immediately issue a recall when it became apparent that the failure rate was higher-than-expected. Plaintiffs allege that the defective design of the DePuy ASR hip has caused them to incur additional medical expenses, suffer severe pain and, in some cases, undergo additional surgery to revise or replace the ASR hip.The DePuy ASR is a metal-on-metal hip replacement system developed in 2005. Health care professionals have increasingly been warning about problems with metal-on-metal hip implants, which can shed metal particles into the body. The particles can damage soft tissue, cause inflammatory reactions and lead to bone loss. The DePuy ASR hip failures appear to be linked to a defective design of the acetabular cup, which is shallower than acetabular cups made by other companies, making it prone to problems.In federal court, a motion has been filed with the U.S. Judicial Panel on Multidistrict Litigation to consolidate and centralize the DePuy ASR recall litigation before one judge for coordinate pre-trial proceedings. As of September 3, when the motion was filed, there were at least five lawsuits over recalled DePuy ASR hip implants pending in five different federal district courts throughout the United States. However, as DePuy hip replacement lawyers continue to review and investigate potential cases for individuals who received one of the recalled implants, it is expected that hundreds, if not thousands, of cases will be filed in different states. Tags: DePuy, DePuy ASR, Depuy ASR Hip, Hip Replacement, Illinois, Indiana, Johnson & Johnson, MDL, Metal Hip Replacement, Metal-on-Metal Hip Image Credit: |More Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 1 Comments Jose August 30, 2012 This interview beetwen Mike and Ben Gordon was excellent!!! Ben pointed out the willful negligence of these manufactures. They know they will sell ten times the amount that they will ever have to pay out in lawsuits. The FDA is complicit in their criminality because Bush/Cheney, as always, stocked the agency that was supposed to protect the consumer with industry insiders. The doctors become just as quilty as soon as they comply with the manufacturer to get signed releases from their patients to cover the corporations ass. It’s just horrible how these people with these implants have suffered needlessly. Once again, in the name of profits and greed. NameThis 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 3 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 4 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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