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.
Heart Rhythm Problems After Transcatheter Aortic Valve Replacement May Have Already Been Present: Study August 13, 2020 Martha Garcia Add Your CommentsThe findings of a new study suggest many reported heart rhythm problems associated with transcather aortic valve replacement (TAVR) surgery may have actually been present in patients before they underwent the heart procedure, raising questions about potential safety concerns previously linked to the procedure.Canadian researchers found that putting an electrocardiogram on patients before they underwent invasive heart surgery allowed them to detect silent heart arrhythmias in more than half of patients.Detecting those arrhythmias led to a change in treatment for nearly one-quarter of patients, and may explain reported problems with arrhythmias previously blamed on TAVR procedures, according to a report published in the August 2020 issue of the journal Cardiovascular Interventions.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 COMPENSATIONThe researchers focused on heart monitoring prior to patients undergoing transcatheter aortic valve replacement surgery (TAVR), whcih is a type of heart surgery that lets a surgeon replace the heart valve by threading it through an artery in the leg instead of during open chest surgery. It places the new valve over the damaged valve.In the past, TAVR surgery has been linked to a high rate of surgical bailout, when a surgeon has to convert to open heart surgery after attempting TAVR, but experiencing complications. In recent years, bailout rates have declined, but patients who have TAVR surgery still face higher rates of death than patients who undergo other procedures.In the latest study, patients wore continuous electrocardiographic monitoring (CEM) devices for seven days sometime within three months prior to undergoing TAVR surgery. The study included 106 patients with severe aortic stenosis and no prior permanent pacemaker.New arrhythmic events (AEs), or events where the heart beat abnormally, were detected by the CEM in 48% of patients. The findings indicate 28% of the patients who had an abnormal heart rhythm needed a change in treatment because of the findings of the CEM.Overall, atrial fibrillation or tachycardia was detected in 10% of patients who did not have known episodes of either. Atrial fibrillation is an irregular or faster heartbeat. Tachycardia is when the heart beats unusually fast, more than 100 beats per minute. This can cause the heart to pump blood less effectively.The data indicates non-sustained ventricular arrhythmias were detected in 29% of patients. Significant bradyarrhythmias, or extremely slow heartbeats, were observed in 21% of patients.These findings lead to treatment change for 36% of patients and 18% of patients then required a permanent pacemaker.Overall, using the CEM led to an increased detection of bradyarrhythimias by up to 30% among patients with pre-existing first-degree atrioventricular blockages and in 47% of patients with pre-existing rich bundle brand blocks, which are various types of blockages in the heart.Research also indicates patients who suffered from chronic renal failure, higher valve calcification and left ventricular dysfunction were more likely to experience arrhythmic events prior to undergoing TAVR surgery. However, new onset arrhythmia events occurred in 22% of patients.The findings are meaningful because of many of the patients may not need TAVR surgery after all, due to other underlying conditions. Early heart monitoring may help prevent many of the risks and complications that may be experienced during TAVR surgeries.Monitoring patients by CEM before TAVR surgery allowed doctors to detect early heart rhythm abnormalities in nearly half of patients and that changed the treatment method for more than one-third of patients.However, the researchers concluded more research is needed to determine how widespread the likelihood may be to help prevent patients undergoing unnecessary surgeries and to help doctors select the right surgery or treatment in each case.โProlonged CEM in TAVR candidates allowed identification of previously unknown AEs in nearly one-half of the patients, leading to prompt therapeutic measures (pre-TAVR) in about one-fourth of them,โ the researchers wrote. โPre-existing conduction disturbances (particularly right bundle branch block) and chronic renal failure were associated with a higher burden of AEs.โ Written by: Martha GarciaHealth & Medical Research WriterMartha 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 Rhythm, Heart Surgery, TAVR, Transcatheter Aortic Valve ReplacementMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 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 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)
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