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.
Bard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026Before thousands of claims were consolidated in a federal MDL, Becton Dickinson indicated that it was reaching individual Bard PowerPort injury resolutions in an average of about 18 months after lawsuits were filed. January 27, 2026 Russell Maas Add Your CommentsWith the first bellwether trials expected to get underway in the Bard PowerPort litigation in April 2026, there is increasing speculation that settlement discussions could intensify over the next few months, to avoid the presentation of evidence that dangerous design defects caused users to experience port catheter fractures, migration and infection injuries. The Bard PowerPort is a totally implantable vascular access device (TIVAD), which has been commonly used in cancer treatment and other long-term therapies, allowing patients to receive chemotherapy, medications or other infusions through a catheter connected to a port placed beneath the skin.To make the catheter visible on imaging scans, Bard incorporated barium sulfate into the material, a design choice that has since been called into question, amid allegations that it can weaken the catheter and increase the risk of devastating injuries.According to lawsuits filed nationwide since 2023, the PowerPort catheter may become brittle and prone to cracking, fissuring or fracturing once implanted. When failures occur, plaintiffs allege the catheter can break free and migrate through the bloodstream, leading to serious complications such as deep vein thrombosis, embolism, infections, organ perforation, cardiac injuries, and in some cases, death.Port Catheter LawsuitDID YOU OR A LOVED ONE RECEIVE AN IMPLANTABLE PORT CATHETER?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.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 Bard PowerPort. Lawsuits are now being pursued by individuals who suffered injuries from the implantable port catheter fracturing or migrating.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAfter a growing number of similar lawsuits raised overlapping questions of fact and law, the federal cases were centralized for coordinated pretrial proceedings in the U.S. District Court for the District of Arizona, where the Bard PowerPort MDL is overseen by Judge David G. Campbell.As of early January, at least 2,545 claims are now pending in the MDL, with additional Bard PowerPort lawsuits continuing to be filed each month. However, the first claim has not yet gone before a jury.PowerPort Settlements Cited Before MDL ConsolidationTo help the parties gauge the relative strengths and weaknesses of their claims, as well as the average Bard PowerPort lawsuit verdicts that juries may return, Judge Campbell has directed the parties to prepare a small group of representative claims for early trial dates, which are scheduled to begin on April 21, July 7, October 13 and December 1, 2026, as well as February 2, 2027.As the start of the first trial gets closer, prior statements by the manufacturers early in the litigation are drawing renewed attention and speculation over whether it will allow evidence to be presented in open court.When the application was submitted to consolidate and centralize all Bard PowerPort lawsuits into an MDL, Becton Dickinson filed a response in opposition, indicating that formal coordination was unnecessary, since it had been successfully resolving claims on an individual basis.In the memorandum (PDF), which was filed in June 2023, the manufacturers indicated that they had previously resolved 11 other Bard implantable port lawsuits within the prior five years, with timeframes ranging from one to 31 months after the claims were first filed. The filing indicates that the Bard PowerPort settlements or resolutions were reached in an average of approximately 18 months, with only one case requiring depositions and none going before a jury.According to the filing, many of those claims involved allegations similar to those now pending in the MDL. Plaintiffs alleged that the radiopaque agent barium sulfate can weaken the catheter when it is not properly encapsulated or separated from the catheter surface, increasing the risk of fractures and related complications.As the size and scope of the litigation grew rapidly after mid-2023, more patients learned their injuries may be linked to design defects in the port catheters, prompting the U.S. Judicial Panel on Multidistrict Litigation to conclude that an MDL was appropriate to coordinate the cases.There are now more than 2,500 lawsuits centralized before Judge Campbell, and lawyers are all closely watching the bellwether trials, to help determine how juries may respond to the evidence and expert testimony that will be repeated throughout thousands of claims.While the outcome of these early bellwether trials will not have any binding impact on other claims, even a small number of plaintiff verdicts could increase the financial exposure faced by the manufacturer, and further increase public awareness about the potential design defects at issue in the lawsuits.Upcoming Bard PowerPort Lawsuit TrialsLast year, Judge Campbell selected six Bard PowerPort lawsuits that will proceed through the bellwether process, with a lawsuit filed by Robert Cook set to be the first that will go before a jury.Cook alleges he was implanted with a Bard PowerPort in September 2023, to facilitate chemotherapy for rectal cancer. However, less than a month later doctors determined the catheter had become infected, requiring intravenous antibiotic treatment.Like other plaintiffs, Cook claims the manufacturers were aware of catheter design problems but failed to adequately warn physicians, patients and regulators about the risks associated with fracture, migration and infection.The Cook bellwether trial is expected to run into early May 2026.Bard PowerPort Lawyers Still Reviewing New CasesIf you or a loved one were injured by an implantable catheter port, submit information about your potential claim for review by a product liability lawyer to determine whether you may be entitled to compensation through a Bard PowerPort lawsuit.Lawyers are investigating cases for individuals who received a PowerPort or other type of implantable port catheter and suffered any of the following injuries:Infections (sepsis or septic shock)Deep vein thrombosis (DVT)Hemorrhaging or bleeding injuriesCardiac/pericardial tamponadeCardiac arrhythmiaSevere and persistent painPerforations of tissues, vessels and organsPatient deathOther injuries caused by fractured PowerPort catheterBard PowerPort injury lawyers provide free case evaluations and there are never any fees or expenses unless a recovery is obtained in your case. Find Out If You Qualify for Port Catheter Compensation Tags: Bard PowerPort Lawsuit, Bard PowerPort Settlement, Catheter Failure, Catheter Fracture, Catheter Infection, Catheter Migration, Port Catheter Settlement, PowerPort Bellwether Trial Image Credit: AdobeStock: 461799104 Written By: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nation’s leading personal injury law firms and oversees the site’s editorial strategy, including SEO and content development.More Bard PowerPort Stories Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims April 16, 2026 Judge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials April 8, 2026 Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection March 31, 2026 0 CommentsLinkedInThis 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: 2 days ago)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 Addict’s ‘Self-Exclusion’ 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: 3 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: 4 days ago)A Florida woman’s 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) Infections After Colonoscopy, ERCP May Result in Lawsuits Over Olympus Scope Problems Patients are developing serious infections after colonoscopy and ERCP procedures, as concerns grow that reusable endoscopes may not be fully… Breast Mesh Implant Complications Often Leave Women Asking If They Have a Lawsuit Women who experienced infection, chronic inflammation, implant instability or other complications after internal bra mesh procedures are now questioning whether… Young People and Gambling: Why Men Are Disproportionately Affected by Sports Betting Addiction As legal sports betting expands nationwide, research and emerging lawsuits suggest that young men face disproportionate risks from mobile sportsbook… The ‘Can’t Feel My Feet’ Symptom Doctors See in Nitrous Oxide Nerve Injury Nitrous oxide injury lawsuits are emerging as medical evidence links recreational use of the gas to nerve damage that can… Cosmetic Surgeons Warn Against Using Internal Bra Mesh for Breast Lifts Plastic surgeons are sounding the alarm over the rising use of mesh-based “internal bra” procedures, warning that the materials may… Sudden Ozempic Blindness Reports Raise Concerns Over NAION Side Effects An increasing number of Ozempic and Mounjaro users are reporting sudden, irreversible vision loss from NAION side effects, prompting new… GalaFLEX Breast Mesh Problems Were Highlighted in Warnings Issued by Former Becton Dickinson Medical Director Former Becton Dickinson safety officer Dr. Hooman Noorchashm warns that the company’s GalaFLEX mesh is being used off-label in breast… Sports Betting Corruption and Addiction Concerns Highlighted By Recent MLB, NBA Player Indictments Federal indictments against MLB and NBA players reveal how legalized sports betting has blurred the line between competition and addiction,… Amazon Fire Pit Safety Warnings Issued to Customers Amid Burn Injury Lawsuits Recall notices are being sent to Amazon customers who purchased tabletop fire pits linked to severe burn injuries, as lawsuits… Internal Bra Mesh Failure Stories Highlight Risk of Pain, Infections and Other Problems Women are sharing alarming reports of pain, infections, and reconstruction failures caused by internal bra mesh implants like GalaFLEX, as… Internal Bra Side Effects Raise Questions About Manufacturers’ Knowledge of Mesh Failures Breast mesh products marketed as “internal bras” for lift and augmentation surgeries are now under investigation amid reports of painful… Dupixent Cancer Risks Outlined in User Stories, as Evidence Mounts of T-Cell Lymphoma Link Dupixent users are coming forward with accounts of devastating cancer diagnoses, saying the popular eczema drug masked early warning signs…
Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection March 31, 2026
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