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.
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.
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.
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.
Dupixent Lawsuit Dupixent lawsuits are being investigated for patients who developed rare blood cancers such as cutaneous T-cell lymphoma (CTCL) after receiving injections, alleging that Sanofi and Regeneron failed to warn about the potential risks of immune suppression and delayed cancer diagnosis.
Tabletop Fire Pit Lawsuit Individuals who suffered severe burns, or families who lost a loved one in a tabletop fire pit explosion, may be eligible for financial compensation through a fire pit injury lawsuit.
Roblox Lawsuit Families are filing Roblox lawsuits after children were targeted by predators for grooming, sextortion, sexual abuse, or exploitation on the platform. Learn who qualifies, what cases allege, and how to file a confidential claim.
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.
Change Healthcare Lawsuit Lawyers are reviewing Change Healthcare class action lawsuits for individuals who had their personal information stolen due to the data breach.
Motion Filed to Consolidate Tylenol Liver Failure Lawsuits in MDL January 21, 2013 Austin Kirk Add Your Comments As a growing number of product liability lawsuits are filed alleging that plaintiffs suffered liver failure from Tylenol side effects, a request has been filed to centralize all federal cases before one judge for coordinated pretrial proceedings as part of an MDL, or multidistrict litigation. Johnson & Johnson faces at least 28 Tylenol liver failure lawsuits filed in U.S. District Courts throughout the country. While the vast majority of them are already pending in the U.S. District Court for the Eastern District of Pennsylvania, there are at least seven other cases pending in different federal courts. All of the complaints involve common allegations that Johnson & Johnson, and it’s subsidiary McNeil Healthcare, sold Tylenol without adequately warning doctors or patients of the risks of liver damage from acetaminophen, the active ingredient found in Tylenol and many other pain medications. Tylenol Autism Lawsuit Does your child have Austism from Tylenol Exposure? Learn More SEE IF YOU QUALIFY FOR COMPENSATION Tylenol Autism Lawsuit Does your child have Austism from Tylenol Exposure? Learn More SEE IF YOU QUALIFY FOR COMPENSATION Tylenol MDL Motion In a motion (PDF) filed with the U.S. Judicial Panel on Multidistrict Litigation (JPML) on January 17, plaintiff Lucky T. Pettersen asked that all complaints filed in federal courts throughout the country be centralized in Pennsylvania to reduce duplicative discovery, eliminate conflicting pretrial rulings from different judges and to increase judicial efficiencies. Pettersen identified at least 28 different complaints that were potential “tag along” actions, which the motion indicates involve common allegations of fact and law. All of the cases have been filed over the past year, and it is expected that the litigation will increase in size over the coming year, as Tylenol injury lawyers are continuing to evaluate and file new cases for individuals diagnosed with liver failure or liver damage. If the cases are consolidated for pretrial procedings, they will be handled in a manner similar to how a Tylenol class action lawsuit would be managed to coordinate discovery and other issues common to all claims. However, the complaints would still remain individual actions, where each plaintiff must establish that the painkiller was defective and the cause of an injury. If an agreement to settle the Tylenol cases is not reached following pretrial proceedings and any potential “bellwether” trials, each claim would ultimately be remanded back to the U.S. District Court where it was initially filed for trial. Lawsuits Allege Failure to Warn About Risk of Tylenol Liver Failure A number of studies have shown links between Tylenol and liver failure. In 1986, acetaminophen was found to be amplified in people with depleted levels of an enzyme known as glutathione, increasing the risk of liver failure. Then, in 1993, studies indicated that acetaminophen liver failure risk was dose dependent and could also be increased by fasting. This was followed by a 1994 label warning indicating that alcohol use also increased the risks of liver failure. 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 a 2002 FDA advisory committee meeting, experts found that there were between 1,000 and 2,000 acetaminophen-induced liver failures each year. In recent years, efforts have been ramped up to bring acetaminophen overdose side effects to the public’s attention and to reduce the amount of liver failure cases linked to the popular analgesic, which is also found in other pain killers and a number of cold medications. In July 2011, McNeil announced that it was lowering the maximum recommended dosage on Tylenol and other acetaminophen-based products from 4,000 mg per day to 3,000 mg per day. The decision came after the FDA announced new limits on acetaminophen levels in prescription painkillers like Vicodin and Percocet. But over-the-counter painkillers and drugs with acetaminophen went unaffected. Tags: Acetaminophen, Johnson & Johnson, Liver Damage, Liver Failure, Pennsylvania, Tylenol More Tylenol Lawsuit Stories Appeals Court Urged To Reinstate Tylenol Lawsuits Over Autism, ADHD Risks September 29, 2025 Tylenol Autism Lawsuits May Get New Life After HHS Pregnancy Warnings September 23, 2025 Study Finds Autism, ADHD Risks Linked to Prenatal Acetaminophen Use August 25, 2025 0 Comments InstagramThis 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 MDL Judge Calls for New Census of Suboxone Tooth Decay Lawsuits (Posted: today) A federal judge has called for a second census of Suboxone tooth decay lawsuits and will require prompt filing of census forms for claims filed from October 1 forward. 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