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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
TAVR Surgery Linked To Increased Endocarditis And Risk of Death: Study May 3, 2021 Russell Maas Add Your CommentsA new study suggests even low-risk patients who underwent transcatheter aortic valve replacement (TAVR) may face an increased risk of death from inflammation developing in the heartโs inner lining, highlighting the importance of routine monitoring following the procedures.The rate of prosthetic valve endocarditis resulting in patient mortality nearly doubled after the first year of implantation, according to the findings of a recent TAVR mortality study presented at the virtual meeting of the Society for Cardiovascular Angiography and Interventions (SCAI) on April 30.TAVR is a type of heart procedure which allows the surgeon to replace the heart valve by threading it through an artery in the leg instead of via open chest surgery. It places the valve over the damaged aortic valve in a less invasive procedure.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONInitially, TAVR was approved for use only among high risk patients who were frail or couldnโt undergo open heart surgery because the surgery carried such high risks. The durability of the heart valves was also untested for use in younger patients, who need implants designed to last 30 years or more, not just 10. However, the occurrence of infections such as Staphylococcus aureus developing around the heart following TAVR procedures has raised concerns.Researchers from MedStar Washington Hospital Center in Washington, D.C. performed an analysis of 396 low-risk TAVR patients to determine the rate of prosthetic valve endocarditis (PVE), which is the development of an infection around the heart valve. PVE can cause a variety of complications including valve leaks, heart blocks, and abscesses, which can result in serious patient injury or death.Of the 396 low-risk patients who underwent TAVR procedures, the incidence of PVE was 1.5% within one year. The rate of occurrence after one year nearly doubled to 2.8%. Researchers noted the survival rates among those with early endocarditis onsets was 100%, while those with late onsets had only a 67% survival rate.Researchers identified 11 patients with PVE, in which three required surgical aortic valve reintervention, while six patients diagnosed with valve endocarditis suffered embolic strokes, two of whom died after antibiotic treatment alone.The study indicates that low-risk TAVR patients are not immune to endocarditis, but researchers caution that these findings are no reason to favor a surgical or transcatheter valve over another during valve replacement.While the studyโs findings have not been published in a peer-reviewed journal and are considered preliminary at this time, prior research has highlighted patient safety risks surrounding TAVR, specifically the increased risk of patient mortality following revision surgeries.In June 2020, University of Washington Medical Center researchers reported patients who underwent a valve-in-valve (ViV) surgery to repair a previous, failed transcatheter aortic valve replacement (TAVR) had lower survival rates and were more likely to need another surgery depending on certain factors, such as the size of the valve.According to the findings, patients wereย more likely to have a failed valve and need surgical intervention if their surgical valves had a smaller internal diameter, they were older, had reduced left ventricular ejection fraction, chronic kidney disease, diabetes, or had surgeons who used a non-transfemoral access during surgery. 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 nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Heart Surgery, Heart Surgery Infection, Infection, TAVRMore Lawsuit Stories Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026 Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges September 10, 2026 LG Electric Range Lawsuit Alleges Defective Controls Caused House Fire September 10, 2026 2 Comments Betty November 23, 2022 This is in reference to my husband Jerald. He started having heart issues in January 2022. He was told in February or March he needed a new heart valve. He had the surgery at Cleveland Clinic in Weston Florida on March 23, 2022. In August he started complaining about back. On Monday November 7, 2022, his blood work was all over the place and had to be admitted to Cleveland Clinic. After a few days we were told he had a very bad infection, possibly caused by his new heart valve. The infection effects his heart, brain and other areas of his body. He has had a stroke. He is now in a rehab hospital. Margaret October 3, 2022 My husband had a Tavr insert and died 3 days later. 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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 Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026) Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)