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.
Tylenol Liver Failure Lawsuit Removed to Federal Court June 5, 2012 Irvin Jackson Add Your CommentsA product liability lawsuit brought against Johnson & Johnson and it’s McNeil unit by a Florida woman who suffered liver failure from Tylenol has been removed to federal court.The complaint (PDF) was originall filed in Florida state court by Charlotte Lee Thompson in February, but late last month Johnson & Johnson had the case removed to the U.S. District Court for the Middle District of Florida based on diversity of citizenship between the company and the plaintiff.According to allegations raised in the Tylenol lawsuit, Thompson developed liver failure in February 2008, after taking Tylenol for several days. Although she indicates that she took Tylenol according to the recommended dose limits, Thompson indicates that her injury was caused by the toxic side effects of the acetaminophen contained in the popular pain killer.Tylenol Autism LawsuitDoes your child have Autism from Tylenol Exposure?Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONTylenol Autism LawsuitDoes your child have Autism from Tylenol Exposure?Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThompson was hospitalized on an emergency basis at Shands Jocksonville Hospital on February 18, 2008, as a result of severe liver damage. She remained hospitalized for more than 10 days with liver failure from Tylenol, according to the complaint.Side effects of acetaminophen have been linked to an increased risk of liver injury and liver failure when the medication is used at high doses.The FDA has indicated that acetaminophen overdose is a leading cause of liver failure in the U.S., resulting in more than 50,000 emergency room visits, 25,000 hospitalizations and over 450 deaths annually. < In recent years, a number of Tylenol liver failure lawsuits have been brought in state and federal courts by individuals who allege that the medication contained inadequate warnings about the risks associated with the medication. Most of the complaints allege that the drug maker failed to warn about the risks of liver failure from overuse of Tylenol or provide information about the consequences of taking multiple medications that contain acetaminophen.Thompson accuses Johnson & Johnson and McNeil Consumer Healthcare of manufacturing, marketing and distributing a defective product, failure to warn and breach of warranty. She is seeking compensatory damages for medical expenses, economic losses as well as physical and emotional injuries. The lawsuit also calls for punitive damages to be leveled against the defendants. Written by: Irvin JacksonSenior Legal Journalist & Contributing EditorIrvin Jackson is a senior investigative reporter at AboutLawsuits.com with more than 30 years of experience covering mass tort litigation, environmental policy, and consumer safety. He previously served as Associate Editor at Inside the EPA and contributes original reporting on product liability lawsuits, regulatory failures, and nationwide litigation trends. Tags: Acetaminophen, Florida, Johnson & Johnson, Liver Damage, Liver Failure, TylenolMore Tylenol Lawsuit Stories Study Questions Link Between Autism and Tylenol Use During Pregnancy January 20, 2026 Study Raises Doubts About Link Between Tylenol and Autism in Children November 25, 2025 Texas Tylenol Lawsuit Accuses J&J of Failing To Warn of Autism Risks October 29, 2025 0 Comments EmailThis 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 Manufacturer Faces Nearly 18,000 Dental Erosion Lawsuits (Posted: today)Indivior faces nearly 18,000 Suboxone dental erosion lawsuits filed by individuals nationwide who say the opioid addiction treatment caused severe tooth damage.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Dry Mouth Lawsuit Claims Dental Problems Could Have Been Avoided With Sublocade Shot (06/18/2026)Suboxone 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) Nevro SCS Lawsuits Warrant Centralization in New MDL: Motion (Posted: yesterday)Plaintiffs have requested that the Judicial Panel on Multidistrict Litigation consolidate all Nevro spinal cord stimulator lawsuits in the Central District of California for pretrial procedures.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITProclaim Spinal Cord Stimulator Lawsuit Follows Infection, Battery Migration Problems (07/06/2026)MDL Sought for Abbott Spinal Cord Stimulator Lawsuits (06/29/2026)Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (06/24/2026) Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (Posted: 2 days ago)An AngioDynamics Vortex port lawsuit alleges the implantable port catheter caused a South Carolina woman to suffer pulmonary embolisms and a serious infection requiring surgical removal.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITAngioDynamics Port Catheter Lawsuit Claims Womanโs SmartPort Implants Caused Multiple Infections (06/23/2026)Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)
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