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.
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Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
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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.
Lawsuit Filed After Bard PowerPort Fractured and Catheter Piece Lodged in Heart Bard PowerPort fractured after it was implanted to administer breast cancer treatments, causing a 5-centimeter catheter piece to lodge in the plaintiff’s heart, which will require additional surgeries to safely remove. August 4, 2023 Irvin Jackson Add Your Comments According to allegations raised in a recently filed product liability lawsuit, dangerous design defects caused a Bard PowerPort to fracture months after it was implanted for chemotherapy injections needed to treat a Texas woman’s breast cancer, causing pieces of the catheter to break off and work its way into her heart. The complaint (PDF) was filed last week by Brandy Songy, in the U.S. District Court for the Eastern District of Texas, pursuing damages from C.R. Bard, Inc., Bard Access Systems, Inc., and their parent company, Beckton, Dickinson and Company, as defendants. The Bard PowerPort is a vascular access device, which is implanted below the skin to provide a catheter port that allows the easy delivery of medications to a patient’s blood stream. It consists mainly of an injection port, where the needle is inserted to deliver medications, and a polyurethane catheter tube which carries the drug into the blood vessel. Unlike other implanted ports, such as Port-a-cath or Mediport, the Bard PowerPort is marketed as a special type of port catheter, which is intended to withstand higher injection pressures. However, Songy now joins a growing number of individuals nationwide who are pursuing Bard PowerPort lawsuits, alleging that the catheter tube is prone to fracture and rupture, which can cause the drugs to leak into the body or result in life-threatening infections, pulmonary embolism, deep vein thrombosis and other complications. Port Catheter Lawsuit DID 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 More SEE IF YOU QUALIFY FOR COMPENSATION Port Catheter Lawsuit DID 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 More SEE IF YOU QUALIFY FOR COMPENSATION According to the lawsuit, Songy received the Bard PowerPort in August 2022, so she could receive breast cancer chemotherapy injections. However, in early last month, in July 2023, Songy underwent emergency heart catheterization after experiencing prolonged episodes of heart palpitation and shortness of breath, and it was discovered tht a five centimeter-long piece of the Bard PowerPort broke off and traveled into her heart. She filed the lawsuit just weeks later, on July 25, 2023. Songy indicated in the complain that she still has to undergo additional surgery to remove portions of the fractured Bard PowerPort that remain in her heart after the first surgery, and will have to undergo further heart evaluations and medical monitoring in the future. According to the lawsuit, Bard knew or should have known of the risk of the PowerPort fracturing, but intentionally concealed those risks from patients and the medical community. “Numerous reports of catheter fractures and migration in the absence of medical provider error were recorded and reported to Defendants before the Device was implanted into plaintiff,” Songy’s lawsuit states. “Despite knowledge of such injuries, Defendants continued to actively and aggressively market the Device as safe. Defendants utilized marketing communications – including the Device’s Instructions for Use and direct communications to Plaintiff’s healthcare providers – to intentionally mislead Plaintiff’s healthcare providers into believing these failures were caused by factors other than catheter design and composition.” Songy’s lawsuit presents claims of negligence, failure to warn, design defect, manufacturing defect, common law fraud, fraudulent concealment, negligent misrepresentation, breach of warranty, violation of the Texas Deceptive Trade Practices Act, and gross negligence. She seeks both compensatory and punitive damages. August 2023 Bard PowerPort Lawsuit Update Given similar allegations raised in other complaints brought throughout the federal court system in recent months, the U.S. Judicial Panel on Multidistrict Litigation (JPML) heard oral arguments last week over whether to centralize and consolidate all Bard PowerPort fracture, rupture and leak lawsuits. Bard has opposed the creation of a PowerPort lawsuit MDL (multidistrict litigation), arguing that each of the claims should continue in different federal courts, without one judge presiding over the common discovery that may impact each claim. The manufacturer suggested it has agreed to pay Bard PowerPort settlements in previously filed lawsuits, indicating that it has been able to resolve claims within an average of about 18 months, usually without any depositions being conducted. However, plaintiffs maintain that the litigation has shifted, and there are now a rapidly growing number of claims being pursued involving very similar allegations. Written by: Irvin Jackson Senior Legal Journalist & Contributing Editor Irvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Bard, Becton Dickinson, Breast Cancer, Catheter, Chemotherapy, Heart, PowerPort Image Credit: | Find Out If You Qualify for Port Catheter Compensation More Bard PowerPort Lawsuit Stories More Than 2,500 Bard Powerport Lawsuits Filed in Federal Courts Nationwide December 5, 2025 Six Bard PowerPort Lawsuits Will Go Before Juries Between May 2026 and Feb. 2027 November 26, 2025 Bard PowerPort Lawsuit MDL Tops 2,000 Cases September 17, 2025 0 Comments FacebookThis 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 No Post Comment I authorize the above comments be posted on this page Weekly 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 Term Δ MORE TOP STORIES Depo-Provera Meningioma Warning Update Approved by FDA, As Lawsuits Move Forward (Posted: yesterday) The FDA has approved an update to the Depo-Provera drug label to include a warning of the risks of meningioma. 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