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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
Atrium C-Qur Hernia Mesh Cases May Now Be Directly Filed in MDL February 20, 2017 Austin Kirk Add Your CommentsThe U.S. District Judge presiding over all federal Atrium C-Qur hernia mesh cases has approved the direct filing of new lawsuits directly into the multidistrict litigation (MDL), which will streamline the process for bringing new product liability claims by individuals nationwide who suffered painful and debilitating complications following hernia repair surgery.ย In December 2016, the U.S. Judicial Panel on Multidistrict Litigation (JPML) consolidated all Atrium C-Qur lawsuits pending in the federal court system, centralizing the cases 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, posing a risk of painful and debilitating complications, such as adhesions, allergic reactions, infections or other problems resulting in the need for removal of the patch months or even years later.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 COMPENSATIONIn a case management order (PDF) issued on February 10, Judge McCafferty indicates that future Atrium C-Qur hernia mesh cases may now be directly filed into the MDL federal court in New Hampshire, which will avoid delays associated with transferring claims from different U.S. District Courts nationwide and promote judicial efficiency.The Atrium C-Qur patch was introduced for hernia repair surgery in 2006, and it has been used during procedures nationwide 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.While there are currently only about two dozen cases pending over problems with Atrium C-Qur, as hernia mesh lawyers continue to review and file claims in the coming months and years, it is expected that hundreds, if not thousands, of lawsuits will be added to the MDL.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. However, if Atrium C-Qur hernia mesh settlements or another resolution is not reached following the MDL proceedings, each individual case may be remanded back to the U.S. District Court where it was originally filed for a separate trial date. Tags: Atrium C-Qur, Atrium Medical, Hernia, Hernia MeshMore Hernia Mesh Lawsuit Stories Bard Ventralex Hernia Mesh Failure Lawsuit Alleges Implant Design Led to Infection October 15, 2026 Covidien ProGrip Mesh Lawsuit Scheduled for March 2027 Jury Trial October 6, 2026 Judge Sets Next Covidien Hernia Mesh Lawsuit for Trial in January 2027 September 11, 2026 0 Comments CommentsThis 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 Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: today)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026) Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: yesterday)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026) Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: 4 days ago)A Georgia womanโs spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)
Dupixent Skin Cancer Lawsuit Filed After Man Diagnosed With Mycosis Fungoides (Posted: today)A man’s Dupixent skin cancer lawsuit claims the eczema treatment led to a CTCL diagnosis.MORE ABOUT: DUPIXENT LAWSUITDupixent Cancer Risks Lead Experts to Recommend Skin Biopsies Before Treatment (10/16/2026)Dupixent Lawyers Seek Leadership Positions in MDL Over Cancer Risks (10/01/2026)Dupixent Side Effects Lawsuit Alleges Drug Caused Cutaneous T-Cell Lymphoma (09/24/2026)
Fujifilm and Olympus Scope Infection Risks Highlight Growing Need for Advanced Disinfection Systems: Report (Posted: yesterday)Concerns about life-threatening infections associated with reusable medical scopes are increasing the need for advanced disinfection technology to protect patients from bacterial contamination.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Medical Device Warning Letter Follows FDA Inspections of Six Manufacturing Facilities (10/16/2026)Olympus Scope Wrongful Death Lawsuit Filed Over ERCP Infection (09/03/2026)Olympus Colonoscopy Lawsuit Over C. Diff Infection Set for Status Hearing in September 2026 (08/27/2026)
Abbott Spinal Cord Stimulator Lead Problems Caused Burning, Shocks, Lawsuit Alleges (Posted: 4 days ago)A Georgia womanโs spinal cord stimulator lawsuit alleges she suffered painful shocks and permanent injuries after an Abbott device’s leads migrated out of position.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITMaster Complaint for Spinal Cord Stimulator Lawsuits Against Boston Scientific to Be Filed (10/12/2026)Abbott and Nevro Spinal Cord Stimulator Lawsuits Centralized in New Federal MDLs (10/05/2026)Spinal Cord Stimulator Lawsuit Alleges Boston Scientific Device Failure Required Removal Surgery (09/29/2026)