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.
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
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.
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.
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.
Short Form Complaints Approved for Filing of Bard IVC Filter Lawsuits December 29, 2015 Austin Kirk Add Your CommentsThe U.S. District Judge presiding over all federal Bard IVC filter lawsuits has approved a procedure to streamline the filing of new cases by individuals who have experienced migrations, perforations or other complications after receiving the device to reduce the risk of blood clots.Since August, all cases filed against C.R. Bard in U.S. District Courts throughout the country involving problems with retrievable inferior vena cava (IVC) filters have been centralized before U.S. District Judge David G. Campbell in the District of Arizona to coordinate discovery, avoid conflicting rulings and to serve the convenience of the parties, witnesses and the courts.There are currently at least six dozen Bard Recovery filter lawsuits, Bard G2 filter lawsuits and other claims involving similar filter designs brought throughout the federal court system.Learn More AboutIVC Filter LawsuitsDesign Problems with Certain IVC Filters Linked to Severe Injuries. Lawsuits Reviewed Nationwide.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutIVC Filter LawsuitsDesign Problems with Certain IVC Filters Linked to Severe Injuries. Lawsuits Reviewed Nationwide.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONEach of the cases involve similar allegations that the small devices implanted to reduce the risk of blood clots traveling to the lungs are defectively designed and unreasonably dangerous, often involving injuries that occurred when a Bard IVC filters migrated or punctured the vein, resulting in severe and often life-threatening health risks.In a case management order (PDF) issued on December 17, Judge Campbell approved the use of a Master Complaint and Short Form Complaint to standardize the process of filing additional lawsuits against Bard directly into the federal multidistrict litigation (MDL).A Master Complaint (PDF) has been adopted by the plaintiffs, which outlines all of the common allegations raised in the various cases. As a result, new plaintiffs filing lawsuits can use a Short Form Complaint (PDF), indicating which specific allegations are adopted, and outlining certain case-specific details involved in their case.The Master Complaint involves counts against C.R. Bard for designing and manufacturing a defective medical device, failure to warn, failure to recall, negligence, negligent misrepresentation, breach of warranty, fraudulent misrepresentation, fraudulent concealment, violating unfair trade practices in various states, loss of consortium, and, in some cases, wrongful death.As Bard IVC filter lawyers continue to review and file additional cases, it is ultimately expected that several thousand lawsuits will be brought in the MDL by individuals throughout the U.S.IVC Blood Clot Filter ConcernsInferior vena cava (IVC) filters are small medical devices that have been implanted in many patients at risk for a pulmonary embolism.The Bard Recovery and G2 filters are two models involved in the lawsuits, which are designed to be retrievable once the risk of a blood clot has passed. However, plaintiffs allege that the manufacturer failed to adequately warn about the importance of removing the filter once the risk of a blood clot has passed, as problems may be more likely to occur the longer the device is in place.In August 2010, the FDA issued aย warning about the risk of IVC filter problems, indicating that the agency had received hundreds of adverse event reports where filters broke free and travelled to other areas of the body or caused other injury.A study published in the medical journalย JAMA Internal Medicineย in March 2013 raisedย questions about the effectiveness of IVC filters, indicating that less than 10% of filters evaluated in the study were successfully removed from patients and 8% of recipients of IVC filters suffered a pulmonary embolism despite the deviceโs presence.In May 2014, the FDA urged doctors to remove IVC filters within about one to two months after the risk of a pulmonary embolism has passed, suggesting that many doctors were not adequately warned about the importance of retrieving the devices.Similar claims have also been raised in Cook Celect and Gunther Tulip IVC filter lawsuits filed over another retrievable design that has been linked to reports of problems. Those cases are consolidated as part of a separate MDL, which is centralized before U.S. District Judge Richard L. Young in the Southern District of Indiana, where a small group of cases are being prepared for early trial dates expected to begin late next year. Tags: Bard G2 Filter, Bard IVC Filter, Bard Recovery Filter, C. R. Bard, IVC FilterMore IVC Filter Lawsuit Stories Gunther Tulip Filter Lawsuit Claims IVC Device Fractured, Punctured Abdomen May 8, 2026 Cook Celect IVC Filter Lawsuit Alleges Device Fractured Into Patientโs Vein February 27, 2026 Lawsuit Alleges Cook Tulip Filter Fractured, Perforated Inferior Vena Cava (IVC) October 31, 2025 0 Comments X/TwitterThis 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 3 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: 4 days ago)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 5 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
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