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.
Atrium C-Qur Hernia Mesh Lawsuit Filing Procedure Streamlined With Master and Short-Form Complaints June 13, 2017 Austin Kirk Add Your CommentsThe U.S. District Judge presiding over all federal Atrium C-Qur hernia mesh lawsuits has approved streamlined procedures for the filing of new cases, involving a “Short Form Complaint” that outlines the allegations from a “Master Complaint” that are being adopted by each plaintiff.In December 2016, the U.S. Judicial Panel on Multidistrict Litigation (JPML) established consolidated pretrial proceedings for all Atrium C-Qur cases brought throughout the federal court system, centralizing the claims before U.S. District Judge Landya McCafferty in the District of New Hampshire to reduce duplicative discovery into common issues, avoid conflicting pretrial rulings and to serve the convenience of the parties, witnesses and the judicial system.Each of the claims raise similar allegations, maintaining that the Atrium C-Qur mesh was defectively designed and unreasonably dangerous for use during hernia repair surgery, causing plaintiffs to suffer painful and debilitating complications, such as adhesions, allergic reactions, infections or other problems, which often result in the need for additional surgery to remove the hernia patch months or even years after it was implanted.Hernia Mesh LawsuitsDid you or a loved one receive a hernia mesh?Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONHernia Mesh LawsuitsDid you or a loved one receive a hernia mesh?Hernia mesh lawsuits are being filed against Bard, Atrium, Covidien and several other hernia mesh manufacturers over mesh failures resulting in injuries and additional surgery.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe Atrium C-Qur patch was introduced in 2006, and has been widely used during hernia repair surgery over the past decade. The polypropylene mesh has an Omega-3 gel coating, which was designed to reduce scar tissue formation while promoting fixation of the mesh to the abdominal wall. However, plaintiffs allege that this coating actually causes severe complications from Atrium CQur mesh, inciting an inflammatory response that promotes bowel adhesion, impedes proper abdominal wall fixation and causes other problems following hernia repair.In a procedural order (PDF) issued on June 12, Judge McCafferty approved a Master Complaint, which outlines all of the various allegations presented in the litigation, and directed each plaintiff with a case already pending to file a Short Form complaint within 60 days.For new Atrium C-Qur lawsuits, Judge McCafferty indicates that plaintiffs can initiate their case by filing the abbreviated form in the District of New Hampshire, which outlines specific information about the individual claim, as well as the counts from the Master Complaint that will be incorporated in their lawsuit.While there are currently only a few dozen complaints centralized before Judge McCafferty as part of the MDL, or multidistrict litigation, as hernia mesh lawyers continue to investigate and file claims for individuals who have experienced problems following surgery where Atrium C-Qur was used, the size of the litigation is expected to rapidly grow over the coming months and years.As part of the coordinated pretrial proceedings, it is expected that Judge McCafferty will establish a โbellwetherโ trial plan, which will select a small group of representative cases for early trial dates to help gauge how juries may respond to certain evidence and testimony that is likely to be repeated throughout the litigation. The use of a Master Complaint and Short Form Complaints will assist the parties and Court in selecting representative cases for eventual bellwether trials.While the outcomes of these early trial dates will not be binding on other claims, the process is designed to facilitate potential hernia mesh settlements that may be necessary to avoid the need for hundreds of individual trials in various U.S. District Courts nationwide following the coordinated MDL proceedings. Tags: Atrium C-Qur, Atrium Medical, Hernia, Hernia MeshMore Hernia Mesh Lawsuit Stories Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients April 21, 2026 Lawsuit Claims Covidien Hernia Mesh Perforated Manโs Bowel April 3, 2026 Parietex ProGrip Hernia Mesh Lawsuit Claims Product Defects Caused Severe Pain After Implantation March 25, 2026 1 Comments Katrina June 24, 2017 I have been having pain like a stabbing whenever I sit , stand or walking sometimes the pain is so bad I try to lay down and keep still but nothing seem to help it , in 2012 I had to have emergency surgery to repair 3 hernias in my abdomen one of them was the size of a golf ball , and about 7 months ago was when the pain was consistent , I had to go out and by pants that were loose fitting and at least 2 sizes to big because I couldn’t have any contact on my stomach and noticed that I haven’t been going to the bathroom like I should sometimes its almost a week or more and my stomach makes so much noise after I eat or drink anything and I will have horrible pain whenever I have to go to the bathroom and then its never much for as long as I have waited to go , so I went to my original surgeon and explained everything as far as the pain to him and he started talking about a scope to find out why im not going like I should and a MRI but I wasn’t able to keep the appointment due to my mom being admitted into the hospital and me having to be there for her , I rescheduled , later having a conversation with someone about this , I was told about getting my hospital records and finding out more about the mesh that was used in the procedure and upon doing so I saw that one of the meshes that was used is having a lot of complications from it and I am hearing people are having the same symptoms and are having to have multiple surgeries to fix the problem so any advice or info on this matter would be helpful 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 Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)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: yesterday)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: 2 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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