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.
Johnson & Johnson Denies Baby Powder Asbestos Contamination, But FDA Stands By Test Results October 30, 2019 Irvin Jackson Add Your CommentsAfter the FDA reported earlier this month that asbestos was found in Johnson’s Baby Powder, Johnson & Johnson claims that its own testing of the same samples has found no evidence of contamination. However, it appears that federal regulators are standing by their test results, which has highlighted serious concerns about the safety of talcum powder products.On October 18, a nationwide Baby Powder recall was issued after the FDA detected sub-trace levels of chrysotile asbestos in the talc-based powder, contradicting years of claims by Johnson & Johnson that their products do not contain the cancer-causing fibers.Johnson & Johnson currently faces thousands of Baby Powder lawsuits, involving allegations that asbestos and talc in the product resulted in the development of mesothelioma, ovarian cancer and other injuries.Learn More AboutTalcum Powder LawsuitsTalcum powder or talc powder may cause women to develop ovarian cancer.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONLearn More AboutTalcum Powder LawsuitsTalcum powder or talc powder may cause women to develop ovarian cancer.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONAlthough evidence uncovered during the litigation has suggested that the manufacturer was aware for decades that asbestos may be present in the talc ingredients, Johnson & Johnson has continued to defend the safety of their popular baby powder, and refused to provide warnings to consumers about the potential cancer risk from talcum powder exposure.In a press release issued on Tuesday, Johnson & Johnson indicates that it had 15 tests conducted on the same sample used by the FDA, and another 48 tests on samples from the same lot it was forced to recall, and claims that they did not find any evidence of asbestos.In response to the claims made by the manufacturer, a report by Reuters News suggests that FDA officials are standing by their own testing and findings.“They would say the product is free of asbestos based on their testing, and we would say the opposite for that sample,” according to a quote provided to Reuters by Steve Musser, the deputy director for scientific operations at the FDA Center for Food Safety and Nutrition.Reuters also revealed that Johnson & Johnson’s claims the sample is asbestos free goes against the findings of one of its own expert witnesses. According to Reuters, it turns out that the private lab which did the testing for the FDA and found the asbestos, was run by Andreas Saldivar, who is a paid expert witness for Johnson & Johnson.Saldivar, director of the laboratory at AMA Analytical Services Inc., did not know he was testing Johnson & Johnson’s Baby Powder when he tested the unmarked sample. He has previously testified in court that Johnson & Johnson’s talc did not contain asbestos.Now, he may be called upon in future cases to testify the exact opposite, particularly since Johnson & Johnson now claims his testing methodologies were faulty and led to the sample becoming contaminated.Johnson & Johnson’s stock price fell sharply earlier this month, over concerns about the liability the company will face in light of the asbestos discovered in talc. Following the press release issued yesterday, the share price has begun to recover, but it remains unclear what impact these findings will have on thousands of lawsuits moving through the federal court system.Johnson & Johnson Talcum Powder LitigationJohnson & Johnson currently faces about 13,000ย product liability lawsuits brought by adult women who allege the developed ovarian cancer, mesothelioma or other injuries following years of exposure to talc in Johnson’s Baby Powder, Shower-to-Shower or other products.While a number of cases have resulted in massive damage awards in state courts, after juries found that there was compelling evidence that Johnson & Johnson failed to warn consumers about the risks associated with their product, most of the claims are currently pending in the federal court system, where a U.S. District Judge is currently considering whether expert witness testimony proposed by plaintiffs is sufficiently reliable to permit the cases to proceed to trial.Last week, plaintiffs attorneys indicated that they intend to supplement prior briefings in light of the FDA discovery that asbestos was found in Johnson’s Baby Powder.If Johnson & Johnson is unable to disqualify plaintiffs expert witnesses in the federal court system, it is expected that a series of โbellwetherโ cases will be scheduled for trial, to gauge how juries respond to certain evidence and testimony that is presented in the federal litigation, and the company will face increasing pressure to consider negotiating talcum powder cancer settlements if they are unable to successfully defend the claims at trial. 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: Asbestos, Baby Powder Recall, Johnson & Johnson, Mesothelioma, Ovarian Cancer, Shower to Shower, Talc, Talcum Powder Image Credit: |More Talcum Powder Lawsuit Stories Additional Talks To Settle Talcum Powder Cancer Lawsuits Set for April 13 March 20, 2026 Ovarian Cancer Talcum Powder Lawsuit Results in $250K Verdict Against J&J February 16, 2026 Evidence That Baby Powder Causes Ovarian Cancer Should Be Admissible At Trial: Report January 22, 2026 0 Comments LinkedInThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: yesterday)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 2 days ago)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: 3 days ago)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
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