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.
DePuy Hip Lawsuits in Federal MDL Growing Quickly December 21, 2010 Staff Writers Add Your CommentsThe number of people filing a lawsuit over recalled DePuy ASR hip replacements has grown quickly in the weeks following a decision to consolidate the federal litigation.ย The U.S. Judicial Panel on Multidistrict Litigation decided to consolidate the DePuy hip recall litigation on December 3rd, assigning all cases filed in courts throughout the United States to Judge David A. Katz in the U.S. District Court for the Northern District of Ohio.At the time the DePuy hip lawsuits were consolidated, there were seven cases transferred to Judge Katz. According to a Conditional Transfer Order filed December 15, in the two weeks since the MDL Panel issued their order, an additional 96 DePuy ASR lawsuits filed in 34 different federal district courts throughout the country were identified. Those cases are also being transferred to Judge Katz’s court for handling during pretrial litigation as part of the multidistrict litigation (MDL).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 COMPENSATIONAll of the complaints contain similar allegations that DePuy Orthopaedics Inc., a subsidiary of Johnson & Johnson, manufactured and sold defective metal-on-metal hip implants, and say that the company failed to warn doctors and patients of the higher-than-acceptable risk that the implants would fail. Many say that the company failed to immediately issue a recall after it became apparent that users were experiencing a higher-than-expected rate of DePuy ASR hip problems.In August, a DePuy hip recall was issued for the ASR XL Acetabular System and the ASR Hip Resurfacing System after the manufacturer acknowledged that the systems had 13% and 12% failure rates, respectively. However, some DePuy recall lawyers suggest the failure rate quoted by DePuy may be conservative, and many more people are likely to be affected by the defective hip replacements.Consolidation of the DePuy hip litigation before one judge as part of an MDL is designed to reduce duplicative discovery, avoid contradictory rulings from different judges and to serve the convenience of the court, witnesses and parties. While the pretrial management of the cases in an MDL is often managed similar to how a class action for the DePuy hip recall would be handled, each claim will still remain an individual lawsuit.If an agreement to settle the DePuy hip lawsuits is not reached following pretrial proceedings and any bellwether jury trials, each of the consolidated cases would be subject to remand back to the jurisdiction where they were originally filed for trial.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. Tags: DePuy, DePuy ASR, Depuy ASR Hip, Hip Implant, Hip Replacement, Johnson & Johnson, Metal Hip Replacement, Metal-on-Metal Hip, Metal-on-Metal Hip Replacement Image Credit: |More Lawsuit Stories Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods April 30, 2026 Weber Grill Brush Lawsuit Claims Detached Bristle Punctured Manโs Intestine April 30, 2026 AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026 6 Comments Lisa April 26, 2015 PLEASE PLEASE RECALL THE S-ROM & THE PRODIGY STEM. IVE HAD BOTH AND THEY WERE BOTH FAILURES. AS I TYPE I SIT HER WITH A PRODIGY STEM BROKEN IN HALF INSIDE MY FEMUR AND I FACE SERIOUS SURGERY WITH PROBABLE BONE DESTRUCTION JUST TO GET LOWER HALF OF STEM… Please please help us. steve March 4, 2011 The s-rom total hip with the metal on metal design should be part of the recall. The acetabular cup is the exact same as the asr and has caused me and my family years of pain and suffering. Why is the ASR and not the S-ROM recalled this is a real bad situation for anyone who has a S-ROM total hip nightmare. The non cemented metal on metal design is the exact same design please answer this for me IT MAKES NO SENCE. I have suffered since 2002 and must take heavy doses of pain medication do to the “CHRONIC PAIN” caused by the flawed S-ROM HIP WITH THE ACETABULAR SHELL. Also what about the metal fliber that are being exposed to our blood exactly like the asr I do believe the entire focus should be on the acetabular cup/shell non cemented this is where the problem is most evident in both the asr and the s-rom systems. PLEASE help out this cause the S-ROM SYSTEM SHOULD BE RECALLED AS WELL AS THE ASR SYSTEMS. karran January 15, 2011 i think we should be albe to represent ourselves for all the suffering i have experienced , i can’t imagine paying an attorney 45 percent, they need to make some kind of law against this, it is greed and a sin. you alre going to do all the work anyway, i have suffered since oct. 08, not the attorney. sometimes you wonder am i still living in America. i hope this judge sends out a message and tells us just exactly how to represent ourselves……. that is while we still have a brain left from all the metal entering our bodies……. Jim January 6, 2011 I had the following S-ROM components implanted 2-22-06; from the operative report: 20x15x165 36 standard neck, +8 lateral stem, with a 20 F XXL sleeve, a 36mm Ultamet, witha 58-mm Pinnacle sector II acetabular cup with no screws, a 36-mm + 9 head. Are any of these components part of the recall? Juergen December 21, 2010 Are you also interested in DePuy Pinnacle Sector II Metal-on-Metal victims? bcuz December 21, 2010 What about the ASR Hip Implants that are not metal to metal, but just the same, had to be replaced? What are we to do? How will we be compensated, even though, they are also failing. Do we just forget about it, because of the Judge’s ruling has decided to limited the Liability. What about us? Where or who do we go to for justice? 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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 Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: yesterday)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 2 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026) Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 3 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)
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