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.
Angiodynamics Xcela Lawsuit Alleges Design Port Defects Caused Severe Infection, Surgical RemovalBarium sulfate used in the port catheter tubes cause Xcela infections and failures, according to lawsuit filed by an Arizona woman who required surgical removal of the port. May 16, 2024 Irvin Jackson Add Your CommentsAngioDynamics faces a product liability lawsuit over Xcela port catheter design defects, indicating that materials used in its construction tend to degrade and cause microfractures, increasing the risk of infections and failure of the port. The complaint (PDF) was filed by Serena Coleman in the U.S. District Court for the Southern District of California on May 9, indicating that she required surgical removal of an AngioDynamics Xcela port after it failed and led to the development of a severe infection.Xcela is a port catheter device that is implanted in patients receiving frequent IV or needle injections. The devices are often used to deliver chemotherapy or other recurrent treatments, involving a port component where a needle can be inserted and a catheter that delivers the fluids directly into a patientโs vein. However, in recent years, design problems with AngioDynamics ports and Bard PowerPort products have lead to questions about the safety of materials used in the construction of the catheter tubes.Coleman now joins a growing number of individuals throughout the United States who are pursuing AngioDynamics port catheter lawsuits against the manufacturers, alleging that the use of high concentrations of barium sulphate makes the catheter tubes prone to cracking or fracturing, which can lead to sever and life-threatening injuries, including sepsis.PORT CATHETER LAWSUITDID YOU OR A LOVED ONE RECEIVE AN IMPLANTABLE PORT CATHETER?Serious and life-threatening injuries have been linked to problems with AngioDynamics port catheters. Lawsuits are being filed by those who suffered injuries from the implantable port catheter fracturing, migrating or causing infections.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONPORT CATHETER LAWSUITDID YOU OR A LOVED ONE RECEIVE AN IMPLANTABLE PORT CATHETER?Serious and life-threatening injuries have been linked to problems with AngioDynamics port catheters. Lawsuits are being filed by those who suffered injuries from the implantable port catheter fracturing, migrating or causing infections.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONColeman indicates that she received an AngioDynamics Xcela port catheter in May 2022. However, in October of that year, she went to a hospital emergency department complaining of central line site pain. Doctors found a lump at the port catheter implant site and determined she suffered from an infection caused by the implant.In late October 2022, Colemanโs infected Xcela port was surgically removed and she blames the infection on the construction of the port catheter with barium sulfate particles.โThis defect in the manufacturing process led to a heterogeneous modified polymer which led to an irregular catheter surface replete with fissure, pits and cracks,โ her lawsuit states. โThe roughened catheter surface leads to the collection and proliferation of fibrinous blood products, thereby drastically increasing the risk of biofilm, infection, and sepsis.โColemanโs complaint indicates she will have to undergo additional surgeries due to the failed port catheter and has suffered permanent injuries as a result. The lawsuit presents claims of negligence, failure to warn, design defect, breach of warranty, fraudulent concealment, and violations of Californiaโs Consumer Legal Remedies Act.Bard PowerPort LawsuitsThe problems described in Colemanโs AngioDynamics Xcela port lawsuit are similar to those made in a growing number of Bard PowerPort lawsuits currently being pursued, which involve similar allegations of design defects.With a rapidly growing number of complaints being filed against Bard throughout the federal court system, the U.S. Judicial Panel on Multidistrict Litigation decided to centralize all Bard Powerport lawsuits in August 2023, transferring the claims to U.S. District Judge David G. Campbell, in the District of Arizona, for coordinated discovery and pretrial proceedings as part of a federal MDL, or multidistrict litigation.To help manage the claims and gauge how juries are likely to respond to certain evidence and testimony that will be repeated throughout the litigation, Judge Campbell has established a bellwether trial process, where a group of 24 initial Bard port catheter lawsuits will go through discovery and be prepared for a series of early trial dates.After the bellwether cases are selected, the parties will conduct further case-specific discovery, including depositions and work up for trial. Those claims will later be reduced down to six Bard PowerPort bellwether trial cases, which will be set to go before juries in late 2025 or early 2026, to help to gauge how they may respond to certain evidence and testimony that will be repeated throughout the litigation.While the outcomes of these early bellwether trials will not have any binding impact on other claims pending in the MDL, they will likely have a major impact on Bard Power Port settlement negotiations and any attempt to resolve large numbers of claims. Tags: Bard PowerPort, Catheter, Catheter Fracture, Infection, Port Catheter, Xcela Port CatheterMore AngioDynamics Port Catheter Lawsuit Stories SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection July 14, 2026 Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026 AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections June 23, 2026 0 CommentsEmailThis 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 Breast Reconstruction Mesh Market Expands Despite Lawsuits Over Synthetic Mesh Failures (Posted: today)Analysts expect wider use of breast reconstruction mesh through 2030, even as lawsuits raise questions about synthetic products, FDA approval and serious complications requiring additional surgery.MORE ABOUT: BREAST MESH LAWSUITGalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (05/26/2026)Galaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026) Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: yesterday)Olympus faces a lawsuit from a Chicago woman who says she developed a severe, life-threatening infection due to the design of its endoscopes, which she says can trap infectious material in their cracks and crevices.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026) Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: 2 days ago)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)
Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism July 7, 2026
AngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections June 23, 2026
Breast Reconstruction Mesh Market Expands Despite Lawsuits Over Synthetic Mesh Failures (Posted: today)Analysts expect wider use of breast reconstruction mesh through 2030, even as lawsuits raise questions about synthetic products, FDA approval and serious complications requiring additional surgery.MORE ABOUT: BREAST MESH LAWSUITGalaFLEX Mesh Problems May Lead Women To Require Breast Implant Removal Surgery (05/26/2026)Galaflex Breast Mesh Lawsuits Filed Against Becton Dickinson in Rhode Island (05/05/2026)Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit (03/05/2026)
Colonoscopy Infection Lawsuit Filed Over Contaminated Olympus Scope (Posted: yesterday)Olympus faces a lawsuit from a Chicago woman who says she developed a severe, life-threatening infection due to the design of its endoscopes, which she says can trap infectious material in their cracks and crevices.MORE ABOUT: SCOPE INFECTION LAWSUITOlympus Scope Infection Concerns Follow Years of FDA Warnings Over Reusable Endoscopes (07/02/2026)Olympus Endoscope Lawsuit Filed Over ERCP Infection, Sepsis Linked to Contaminated Scope (06/09/2026)Pediatric Sepsis Cases Contribute to More Than 1,800 Childrenโs Deaths Annually in U.S.: Study (03/31/2026)
Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (Posted: 2 days ago)A Boston Scientific spinal cord stimulator lawsuit claims the chronic pain implants are defectively designed, causing a Louisiana woman to suffer shocks and pain, as well as dizziness and fainting spells.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro SCS Lawsuits Warrant Centralization in New MDL: Motion (07/08/2026)Proclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)