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.
Lawsuit Alleges Angiodynamics Vortex Chemo Port Catheter Broke During RemovalBroken pieces of the Angiodynamics Vortex chemo port have been deemed too dangerous to remove from the plaintiffโs veins. September 27, 2024 Irvin Jackson Add Your CommentsA New Jersey man has filed a lawsuit over problems with the AngioDynamics Vortex chemo port, indicating that the catheter broke when doctors tried to remove it, leaving behind debris that has migrated through his body, causing severe injuries. The AngioDynamics Vortex port catheter system was approved by the U.S. Food and Drug Administration (FDA) in 2003. It was originally called the Triumph VTX port and was created by Horizon Medical Products, which was later acquired by AngioDynamics. It allows long-term access to the vascular system to deliver medications, nutrients and treatments, such as chemotherapy, directly into a patientโs bloodstream.While the AngioDynamics Vortex has been marketed as a safe and effective medical device, a number of lawsuits over the chemo port now allege that the system was defectively designed, creating a risk of failure, migration and infection injuries, due to materials used in the catheter that weaken the structural integrity of the devices.The allegations are similar to those made in a series of Bard PowerPort lawsuits being pursued against C.R. Bard, each indicating that the chemo port is prone to fracturing, migrating and causing infections due to the breakdown of barium sulfate used during the manufacturing process.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 COMPENSATIONGiven nearly identical allegations raised in the complaints brought against Bard throughout the federal court system, the U.S. Judicial Panel on Multidistrict Litigation (JPML) 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.However, the AngioDynamics chemo port lawsuits are not included in this consolidation, and continue to be spread out in different U.S. District Courts nationwide.AngioDynamics Vortex Lawsuits Could Also Be Centralized in MDLJeremy Matchett filed a new complaint (PDF) over the AngioDynamics Vortex port on September 24, in the U.S. District Court for the Eastern District of Pennsylvania, indicating that a portion of his chemo port broke while doctors were attempting to remove it, and portions remained in his body for months, unbeknownst to him or his doctorsAccording to the lawsuit, Matchett had a previous port catheter removed and replaced with an AngioDynamics Vortex chemo port in August 2018, as part of his treatments for chronic myeloid leukemia.In May 2023, doctors determined that the chemo port was no longer needed, and attempted to remove it. However, they found the device was difficult to remove, and a portion of the catheter broke off.Healthcare professionals were unaware that the remaining fragments of the broken Vortex port remained in Matchettโs body until August 2023, when he began complaining of chest pain and palpitations whenever he lay on his left side. During treatment, a CT scan revealed that a fragment of the broken chemo port had migrated to his left brachiocephalic vein.โDue to the location of the retained fragment and the risk to Plaintiff for an attempted removal of the fragment, the decision was made to leave the retained Vortex fragment in Plaintiffโs body,โ the lawsuit states. โTo date, the retained fragment of the Vortex remains in Plaintiffโs left brachiocephalic vein.โMatchett presents claims of negligence, failure to warn, design defect, breach of warranty, fraudulent concealment and violations of Pennsylvania consumer protection laws, naming AngioDynamics Inc. and Navilyst Medical Inc. as the defendants.The complaint was filed just two days before the JPML is set to hear oral arguments over whether to establish a separate MDL for all federal lawsuits over AngioDynamics port catheters.Similar to the Bard PowerPort lawsuits, if an MDL is established, complaints brought against AngioDynamics in U.S. District Courts throughout the country will be transferred to one judge for discovery, pretrial proceedings and potentially a series of early bellwether trials. However, if the parties fail to reach an AngioDynamics port catheter settlement agreement or another resolution during the MDL proceedings, each lawsuit may be transferred back to their originating districts for individual trial dates in the future. Tags: Angiodynamics, Catheter Fracture, Catheter Migration, Chemo Port, Implantable Port Catheter, Vortex Port CatheterMore AngioDynamics Port Catheter Lawsuit Stories AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims April 16, 2026 Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots April 9, 2026 1 Comments Patrick October 13, 2024 This is unacceptable from these companies.. these people are already dealing with a ton on their plate to worry about this type of negligenceInstagramThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: yesterday)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 2 days ago)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: 3 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)
AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026
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