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.
Talcum Powder Asbestos Documents Requested By Congressional Committee, As J&J CEO Skips Out On Hearing December 13, 2019 Irvin Jackson Add Your CommentsThe head of Johnson & Johnson refused to testify at a U.S. House of Representatives subcommittee hearing this week, which was examining the detection of asbestos in talcum powder, and a leading House Democrat demands Johnson & Johnson turn over documents about what the company knew regarding asbestos in talc, and when it knew it.On December 10, the House Subcommittee on Economic and Consumer Policy held a hearing on carcinogens in talc and the best methods for asbestos detection.The hearing comes after Johnson & Johnson was forced to issue a Baby Powder recallย that impacted tens of thousands of bottles on October 18. The action was taken after the FDA detected sub-trace levels of chrysotile asbestos in Johnson & Johnson talcum powder, contradicting years of claims by the manufacturer that their popular Baby Powder does not contain the cancer-causing fibers.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 COMPENSATIONHouse Democrats on the committee invited Johnson & Johnsonโs Chief Executive Officer Alex Gorsky to attend, but he refused. The company indicated that it thought the hearing was unfair, due to the involvement of testimony by experts who are also testifying against the company in ongoing litigation brought by consumers diagnosed with cancer following use of talc powder.Johnson & Johnson faces about 13,000ย Baby Powder lawsuitsย andย Shower-to-Shower lawsuitsย that are pending in the federal court system, which involving similar allegations that women were diagnosed with ovarian cancer, mesothelioma or other injuries that were allegedly caused by regular exposure to talcum powder, which was commonly applied to their bodies on a regular basis for decades.Although evidence uncovered during the litigation suggests the manufacturer has been aware for decades that asbestos may be present in the talc ingredients, increasing the risk of cancer, Johnson & Johnson has attempted to defend the safety of their popular baby powder, and refused to provide warnings to consumers about the potentialย cancer risk from talc-based powder.Subcommittee Chair Raja Krishnamoorthi said he was disappointed in Gorskyโs refusal to appear and defend his company in the face of growing evidence of the presence of asbestos in its talcum powder products.โThereโs evidence that for decades tests have repeatedly found that Johnson & Johnsonโs talc-based Baby Powder contained asbestos,โ Krishnamoorthi said in his opening statement. โMore sensitive testing methods than those used by Johnson & Johnson have detected asbestos in talc.โRepresentative Krishnamoorthi questioned why the company has refused to put a cancer label warning on talc-based products, why it appeared to specifically target minorities in its advertising after internal concerns were raised about the possible presence of asbestos, and why it prominently labels its cornstarch-based productsโ primary ingredient, but does not do the same for those based on talc.On the same day, Representative Krishnamoorthi sent a letter (PDF) to Gorsky, requesting documents and information โconcerning recent public statements made by Johnson & Johnson casting doubt and sowing consumer confusion about the detection of asbestosโ in Baby Powder by the FDA.The Representative is seeking documents on the companyโs decision to limit the recall to just one lot, public statements made following the October 18 recall, itโs response to the FDA regarding the recall, testing data, information on mines and manufacturing facilities, and a number of other marketing decisions.Talc Asbestos Testing Methods QuestionedA number of witnesses testified at the hearing, including William E. Longo, who has a doctorate in Materials Science and Engineering, and is president of Materials Analytical Services LLC. In his testimony (PDF), Longo questioned Johnson & Johnsonโs use of what he describes as less-sensitive testing methods.โIndependent labs throughout the country and over the course of several decades have documented the presence of asbestos in consumer talcum products including Johnson’s Baby Powder. AMA Analytical, Forensic Analytical, MVA Scientific Consultants, our own lab MAS, and Johnson & Johnson’s own consultants โ Colorado School of Mines, Dartmouth University, McCrone Associates, Rutgers University, The RJ Lee Group (and others) have all documented asbestos in Johnson’s and other manufacturersโ talcum products over the course of decadesโ he testified. โThe cosmetic talc industry has, in that time, accumulated hundreds, if not thousands of testing results that report โno detectable or quantifiable asbestos.โ These reports, regarded by the manufactures as โnegative,โ are very misleading as they result from analytical and methodological techniques with poor detection limits.โWhen the FDA first announced finding asbestos in one batch of Baby Powder, just 11 days later, Johnson & Johnson announced that its own independent testing found no traces of asbestos in the talcum powder. However, the company then acknowledged that it had to redo the testing, after evidence suggested that it was rushed and that the company tossed some results showing the presence of asbestos, claiming that data was tainted. The company now maintains that the new tests still show no signs of asbestos.The FDA finding evidence of asbestos contamination in current bottles of Johnson Baby Powder distributed to stores throughout the U.S., is likely to have a major impact on the on-going litigation, and undercut the manufacturerโs defense.While a number of cases have already 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.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 negotiatingย talcum powder cancer settlementsย 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, Cancer, Congress, 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 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 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: yesterday)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston 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)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 2 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone 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)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 3 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
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