AirTag Tracking Lawsuit Claims Apple Failed to Provide Adequate Stalking Safeguards for iPhone, Android Users
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.
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
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.
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.
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 FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses August 19, 2026 AirTag Tracking Lawsuit Claims Apple Failed to Provide Adequate Stalking Safeguards for iPhone, Android Users August 19, 2026 Anti-Seizure Drugs Linked to a Quarter of Stevens-Johnson Syndrome Cases August 19, 2026 0 Comments URLThis 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 FanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (Posted: yesterday)A FanDuel addiction lawsuit claims a Pennsylvania man wagered massive amounts of money after being subjected to a tailored promotional campaign designed to exploit his gambling habits.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITDraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026)Lawsuit Claims FanDuel, DraftKings Caused Compulsive Gambling, Addiction and Financial Losses (07/24/2026) Boston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (Posted: 2 days ago)A spinal cord stimulator lawsuit from a Kentucky man claims his Boston Scientific device was defectively designed, leaving him with permanent nerve damage and wire fragments fused into his bones.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026)Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026) Covidien Mesh Lawyers to Meet With MDL Judge This Week, Following Landmark Verdict (Posted: 3 days ago)A federal judge has called for a meeting between attorneys representing plaintiffs and defendants in Covidien mesh lawsuits following an $88 million verdict against the manufacturers.MORE ABOUT: HERNIA MESH LAWSUITCovidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (08/05/2026)Hernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)
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