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.
Rapid Deterioration of TAVR Heart Valves Seen in Some Kidney Disease Patients: Study One-in-four patients with end-stage kidney disease experienced rapid deterioration of TAVR heart valves within just six months of implantation. May 22, 2023 Martha Garcia Add Your Comments A new study highlights a potential risk from TAVR (transcatheter aortic valve replacement) surgery for individuals suffering from kidney disease, indicating that some of these patients may experience rapid deterioration of their heart valves. More than one-quarter of patients with end-stage renal disease suffered rapid deterioration of TAVR heart valves, according to findings presented at the Society for Cardiovascular Angiography and Interventions annual meeting. Research presented at a conference is considered preliminary until published in a peer-reviewed journal. TAVR is a type of heart surgery that 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, which is why it is often favored by doctors, but can carry its own risks. End-stage renal disease, or kidney failure, is the gradual loss of kidney function. The kidneys stop filtering waste and excess fluid from the blood, requiring dialysis for treatment. TAVR Valve Deterioration Risks Researchers conducted a single-center study including 95 consecutive end-stage renal disease patients who had TAVR for aortic stenosis at the Henry Ford Hospital in Detroit, Michigan, from 2012 to the present. Cases of infective endocarditis, valve thrombosis, and patient-prosthesis mismatch were excluded. Of the kidney failure patients, 10 suffered valve events within six months of having a TAVR placement. Those patients suffered structural valve degeneration; a breakdown of the structure of the heart valve. Kidney disease patients experienced rapid deterioration of the transcatheter aortic valve, but the data indicated the need for reintervention or repeat TAVR surgery wasnโt common, despite the deterioration. Roughly 3% of patients had reintervention compared to rates of intervention after SAVR surgical replacement, another type of valve replacement, at 2% to 7%. The rate of valve degeneration increased steadily over the follow-up period after TAVR surgery, the researchers found. Valve degeneration occurred within one year on average, but most often occurred within two years. In 12% of cases, valve degeneration occurred by aortic stenosis and in 16% of cases by aortic regurgitation. Overall, rates of side effects, cardiac events, and long-term major adverse events were high among patients. TAVR Health Concerns Other research indicates even low-risk patients who undergo TAVR surgery face an increased risk of death due to inflammation in the heartโs inner lining. Inflammation is a risk posed to all TAVR patients, whether low or high risk and may be a risk factor for valve degeneration as well. Do You Know about… Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ Spinal Cord Stimulator lawsuits Spinal 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 More SEE IF YOU QUALIFY FOR COMPENSATION Despite the high risk of valve degeneration, these patients already face a risk of suffering complications, like valve disease, and death, which may be part of what contributes to the increased risk of valve degeneration, the researchers warn. Another study published in 2021 concluded patients who undergo an emergency second TAVR surgery face an increased risk of severe bleeding events, strokes, and death. Patients who need TAVR face a significant risk of suffering other side effects. Many patients with high-risk factors may be too high risk to undergo valve reintervention surgery to repair the valve, allowing the degeneration to progress, the researchers concluded, indicating it is important to determine which patients may be too sick to treat and who can undergo reintervention to help repair degeneration. Written by: Martha Garcia Health & Medical Research Writer Martha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Heart Surgery, Heart Valve, Kidney Disease, TAVR More Lawsuit Stories Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain April 3, 2026 Lawsuit Claims Covidien Hernia Mesh Perforated Manโs Bowel April 3, 2026 Judge Upholds $9M Crock-Pot Pressure Cooker Lawsuit Verdict April 3, 2026 0 Comments PhoneThis 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 Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: yesterday) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026) Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 2 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026) Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: 3 days ago) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)Court Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)
Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (Posted: yesterday) An Illinois woman has joined a growing number of plaintiffs alleging that the Medtronic Intellis neurostimulator, and similar devices, may fail to relieve chronic pain and instead lead to worsening complications. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)Abbott Proclaim SCS Lawsuit Alleges Stimulator Lead Migration Resulted in Multiple Surgeries (03/24/2026)Abbott, Boston Scientific Oppose Spinal Cord Stimulator Lawsuit MDL (03/20/2026)
Court Outlines Plan To Prepare Suboxone Tooth Decay Lawsuits for Trial in Early 2028 (Posted: 2 days ago) Four Suboxone tooth decay lawsuits will eventually be selected and prepared for bellwether trials set to begin in March 2028, according to a court order. MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Film Lawsuit Filed by 46 Users Alleging Drug Makers Ignored Years of Dental Injury Reports (03/03/2026)100 Suboxone Film Tooth Decay Lawsuits Selected for Next Phase of Bellwether Discovery (02/13/2026)Problems With Suboxone Dental Injury Records Collection Continues in MDL (01/26/2026)
Hair Relaxer Class Action Lawsuit Seeks Certification for Medical Monitoring Claims (Posted: 3 days ago) A federal judge is being asked to certify seven hair relaxer class action lawsuits seeking medical monitoring for users, following studies that link the products to an increased risk of cancer. MORE ABOUT: HAIR RELAXER LAWSUITHair Relaxer Endometrial Cancer Lawsuits and Ovarian Cancer Lawsuits Proposed for Early Trials (03/23/2026)Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (03/12/2026)Court Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)