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.
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.
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.
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.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
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.
AngioDynamics Port Catheter 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.
Processed Food Lawsuit Lawsuits are being pursued against the food industry over their manufacturing and advertising of ultra-processed foods, which have caused a generation of children to face an increased risk of developing childhood diabetes and other chronic illnesses.
Bard Port Catheter Lawsuit Alleges PowerPort Device is Defective, Unreasonably Dangerous This is the latest of several Bard PowerPort catheter lawsuits filed in recent weeks; all claiming the catheter tube is defective and can erode and crack. May 16, 2023 Irvin Jackson Add Your Comments A Missouri man has filed a product liability lawsuit alleging that a Bard port catheter device, known as the Bard PowerPort, was defectively designed and caused him to develop a severe fungal infection. The complaint (PDF) was filed by Vincent Anderson on May 9 in the U.S. District Court for the Western District of Missouri, presenting claims against Becton, Dickinson and Company, C.R. Bard, Inc., and Bard Access Systems, Inc., calling for both damages and for the Bard port catheter be recalled from the market. 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, Anderson now joins a growing number of individuals nationwide who are pursuing Bard PowerPort lawsuits, alleging that the catheter tube is prone to crack and fracture, increasing the risk of infections, deep vein thrombosis and other complications. Bard Port Catheter Lawsuit Did you or a loved one receive a Bard Powerport? 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 Bard Port Catheter Lawsuit Did you or a loved one receive a Bard Powerport? 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 complaint, Anderson had the Bard port implanted into his right internal jugular vein in March 2020 to receive injections of chemotherapy drugs to treat his urothelial cancer. However, he was readmitted to the hospital in December 2021 because the PowerPort had developed a fungemia infection. The infected Bard port catheter was removed and Anderson was placed on an antifungal medication. “Defendants misrepresented the safety of the PowerPort system, and negligently designed, manufactured, prepared, compounded, assembled, processed, labeled, marketed, distributed, and sold the PowerPort system as safe and effective device to be surgically implanted to provide repeated access to the vascular system for the delivery of medications, intravenous fluids, parenteral nutrition solutions, and blood products,” the lawsuit states. “Defendants knew and had reason to know, that the PowerPort was not safe for the patients for whom they were prescribed and implanted, because once implanted the device was prone to surface degradation and resulting thromboembolism, infection, mechanical failure, and a variety of other complications.” Similar to other port catheter lawsuits, Andersons claim states that soon after the Bard implantable port catheter was introduced to the market, the manufacturers began receiving reports of PowerPort problems, mostly concerning thromboembolism after implantation. These also involved injury reports including: Hemorrhage Infection and sepsis Cardiac/pericardial tamponade Cardiac arrhythmia Severe and persistent pain Perforation of organs, tissues and blood vessels Death The lawsuit claims the manufacturers could have changed the design to make it safer for patients, but instead continued to aggressively market the device in order to maximize profits at the expense of potential patient injuries. Anderson alleges the manufacturer’s actions constitute “willful, wanton, gross and outrageous corporate conduct”, since they failed to provide adequate warnings; failed to establish adequate post-marketing surveillance systems, and failed to issue a Bard PowerPort recall after discovering the defects associated with the device. Find Out If You Qualify for Port Catheter Compensation Tags: Bard, Becton Dickinson, Catheter, Deep Vein Thrombosis, Embolism, Fungal Infection, PowerPort 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. More Bard PowerPort Lawsuit Stories Bard PowerPort Infection Lawsuit Chosen for First Bellwether Trial in Feb. 2026 July 18, 2025 More Than 1,700 Bard PowerPort Lawsuits Now Filed in State and Federal Courts June 3, 2025 6 Bard PowerPort Lawsuits Selected for Bellwether Trials in Federal MDL May 19, 2025 0 Comments 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 TermEmailThis field is for validation purposes and should be left unchanged. Δ MORE TOP STORIES Depo-Provera Brain Tumor Caused Numbness Over Half of Woman’s Body, Lawsuit Alleges (Posted: yesterday) A Depo-Provera brain tumor lawsuit indicates it took years for a woman to learn that her condition was linked to the birth control injections. 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