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.
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.
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.
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.
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.
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.
Ocaliva Lawsuit Ocaliva lawsuits are being investigated for users who experienced liver failure, cirrhosis progression, transplant, or death after taking the drug, alleging that Intercept Pharmaceuticals failed to warn about the risk of dosing toxicity and accelerated liver damage.
ByHeart Formula Recall Lawsuit Parents are now filing ByHeart recall lawsuits alleging that contaminated infant formula caused botulism and other serious illnesses after the company failed to prevent or warn about dangerous manufacturing lapses.
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.
Discovery Plan Issued for Tylenol Injury Lawsuits in MDL October 3, 2013 Austin Kirk Add Your Comments The U.S. District Judge presiding over all federal Tylenol liver injury lawsuits has issued a preliminary discovery plan for the coordinated pretrial proceedings in the Multidistrict Litigation (MDL). Earlier this year, the U.S. Judicial Panel on Multidistriction Litigation (JPML) established a Tylenol MDL for all complaints filed in U.S. District Courts nationwide alleging that users suffered liver damage or liver failure following use of Tylenol. The cases are centralized before U.S. District Judge Lawrence F. Stengel in the Eastern District of Pennsylvania to reduce duplicative discovery, avoid conflicting pretrial rulings and to serve the convenience of the witnesses, parties and courts. Tylenol Autism Lawsuit Does your child have Autism from Tylenol Exposure? Learn More SEE IF YOU QUALIFY FOR COMPENSATION Tylenol Autism Lawsuit Does your child have Autism from Tylenol Exposure? Learn More SEE IF YOU QUALIFY FOR COMPENSATION As the number of Tylenol injury cases in the MDL continues to increase, the organization and structure of the pretrial proceedings are being established. A small group of lawyers have been appointed to serve in leadership roles in the litigation, and Judge Stengel is expected to schedule a tutorial day so that the parties may educate the Court on the science that will be involved in the cases and provide information about the link between Tylenol and liver failure. On October 1, Judge Stengel issued a Case Management Order (PDF) which establishes the preliminary discovery plan for the Tylenol litigation. While the plan provides no firm dates or projections of when the first Tylenol trials will begin, it lays out the ground rules for generic discovery that applies to all cases, the development of fact sheets to be exchanged between the parties and the coordination of pretrial proceedings with state court actions. The parties have been ordered to meet within the next 10 days to resolve some existing disputes over the discovery process, including a claim by plaintiff attorneys that Johnson & Johnson has failed to respond adequately to prior discovery requests. Tylenol Liver Injury Problems There are currently at least 80 product liability lawsuits pending before Judge Stengel involving claims that side effects of Tylenol caused liver injuries. However, as additional cases are filed throughout the federal court system they will be transferred to the MDL for coordinated pretrial proceedings. It is ultimately expected that hundreds, if not thousands, of cases will be brought alleging that inadequate warnings were provided about the link between Tylenol and liver problems. Tylenol is one of the most widely used painkiller medications in the United States, which has been used by millions of Americans. The medication contains acetaminophen as the active pharmceutical ingredient, which has been identified in recent years as a leading cause for liver injury in the United States. The FDA has indicated that acetaminophen may be responsible for more than 50,000 emergency room visits each year, including 25,000 hospitalizations and over 450 deaths annually. In recent years, efforts have been ramped up to bring the risk of acetaminophen overdose to the public’s attention and to reduce the amount of liver injury cases linked to the popular analgesic, which is also found in other pain killers and a number of cold medications. Johnson & Johnson lowered the maximum recommended dosage on Tylenol and other acetaminophen-based products from 4,000 mg per day to 3,000 mg per day in 2011 after the FDA announced new limits on acetaminophen levels in prescription painkillers like Vicodin and Percocet. However, the lawsuits allege that the drug maker has withheld important safety information from the public for decades, ignoring the narrow window between the recommended dosage for Extra Strength Tylenol and the risk of liver injury. Judge Stengel has scheduled a series of status conferences in the Tylenol MDL through the end of the year, and it is expected that a small group of cases will eventually be selected for early trial dates, known as “bellwether” trials. The preparation and outcomes of these cases are designed to help facilitate potential Tylenol settlement agreements or another resolution for the litigation. Tags: Acetaminophen, Johnson & Johnson, Liver Damage, Liver Failure, Tylenol More Tylenol Lawsuit Stories 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 Tylenol Autism Warnings Challenged by J&J Spinoff Kenvue October 23, 2025 0 Comments CompanyThis 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 Breast Mesh Malpractice Lawsuit Claims Use of Unapproved Internal Bra Caused Complications (Posted: today) A Florida surgeon is standing trial over allegations that he implanted unapproved VentriO breast mesh without consent, causing severe infections, permanent nerve damage, and multiple reconstructive surgeries. 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