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.
Pacemaker and Implantable Defibrillator Complication Rates Appear Hospital-Specific, Study Finds August 7, 2019 Martha Garcia Add Your CommentsComplication rates with pacemakers and implantable defibrillators often vary widely based on the hospital where the procedure occurred, according to the findings of a new study.In a report published last week in the Annals of Internal Medicine, Australian researchers indicate that one of the biggest factors impacting the implantable defibrillator complication rates may be the hospital where they were implanted.Cardiac implantable electronic devices (CIEDs) include permanent pacemakers, implantable cardioverter defibrillators, and cardiac resynchronization therapy devices. They are used to keep a patientโs heart continuously beating after suffering a serious cardiac event, such as heart attack or other problem that required continued electrical stimulation.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 COMPENSATIONResearchers from the University of Adelaide in Australia looked at data from 174 hospitals in Australia and New Zealand. Of those, 98 hospitals implanted at least 25 or more CIEDs during the study period from 2010 to 2015.The data involved 81,300 patients ages 18 or older; 40% of whom received a new CIED. More than 65,000 received permanent pacemakers and nearly 16,000 received implantable cardioverter defibrillators (ICDs).Overall, 8% of patients who received a CIED of any kind suffered a major complication or side effect within 90 days of the operation. Roughly 60% occurred after the patient left the hospital.Complication rates differed between 2- and 3-fold among different hospitals. Complication rates for implantable cardioverter defibrillators were 10%, compared to permanent pacemakers at 7%. However, 76% of complications were attributed to permanent pacemakers, since they are implanted in much larger numbers.The study indicates complication rates just for permanent pacemakers varied from 5% to 13% and complication rates for implantable cardioverter defibrillators ranged from 6% to 17%.Researchers determined the widely differing complication rates suggest hospital care also varies widely. The average complication rate was 8%, but the complication rates varied from 5%to 14%. According to the data, 22 hospitals were identified as having complication rates that were significantly different from the national average.Prior studies have shown CIEDs are beneficial to patients and carry small complication risks ranging from 3 to 6%. However, researchers warn the findings of those studies donโt account for the change in quality of care from one hospital to another, since they are from large clinical trials. Instead, they claim the new research reveals more accurate complication rates. 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: Defibrilator, Heart Implants, PacemakerMore Lawsuit Stories Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot June 18, 2026 Meta Faces Lawsuit Over Sports Betting Ads on Facebook, Instagram June 18, 2026 Nexgrill Class Action Lawsuit Alleges Manufacturer Botched Grill Brush Recall June 18, 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 Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (Posted: today)Five plaintiffs say they all suffered dental problems due to the side effects of Suboxone, which could have been avoided with adequate warnings.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (06/11/2026)Suboxone 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) Lawsuit Claims Dupixent Cancer Diagnosis Occurred After Only 8 Months of Use (Posted: yesterday)The makers of Dupixent face a CTCL lawsuit by a man who says he developed the rare form of cancer less than a year after beginning treatment with the eczema drug.MORE ABOUT: DUPIXENT LAWSUITRezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis (06/12/2026)Dupixent Injection Lawsuits Consolidated in MDL Over CTCL Diagnoses (06/09/2026)Dupixent Injection Lawsuit Alleges Manufacturer Failed to Warn About T-Cell Lymphoma Cancer Side Effects (06/04/2026) Abbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (Posted: 2 days ago)Four plaintiffs allege Abbott spinal cord stimulator battery problems, painful malfunctions and other device failures caused worsening symptoms and repeat surgeries after the company made hundreds of changes to its implant systems.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston 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)
Suboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot June 18, 2026
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