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.
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.
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.
AngioDynamics Port Catheter 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.
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.
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.
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.
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 Comments The 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 recall 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 About Talcum Powder Lawsuits Talcum powder or talc powder may cause women to develop ovarian cancer. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Learn More About Talcum Powder Lawsuits Talcum powder or talc powder may cause women to develop ovarian cancer. Learn More SEE IF YOU QUALIFY FOR COMPENSATION House Democrats on the committee invited Johnson & Johnson’s 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 13,000 Baby Powder lawsuits and Shower-to-Shower lawsuits 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 potential cancer risk from talc-based powder. Subcommittee Chair Raja Krishnamoorthi said he was disappointed in Gorsky’s refusal to appear and defend his company in the face of growing evidence of the presence of asbestos in its talcum powder products. “There’s evidence that for decades tests have repeatedly found that Johnson & Johnson’s talc-based Baby Powder contained asbestos,” Krishnamoorthi said in his opening statement. “More sensitive testing methods than those used by Johnson & Johnson have detected asbestos in talc.” Representative 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 products’ 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 “concerning recent public statements made by Johnson & Johnson casting doubt and sowing consumer confusion about the detection of asbestos” in Baby Powder by the FDA. The Representative is seeking documents on the company’s decision to limit the recall to just one lot, public statements made following the October 18 recall, it’s 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 Questioned A 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 & Johnson’s use of what he describes as less-sensitive testing methods. “Independent 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 – 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 manufacturers’ talcum products over the course of decades” he testified. “The cosmetic talc industry has, in that time, accumulated hundreds, if not thousands of testing results that report “no detectable or quantifiable asbestos.’ These reports, regarded by the manufactures as ‘negative,’ are very misleading as they result from analytical and methodological techniques with poor detection limits.” When 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 manufacturer’s 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 “bellwether” 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 Jackson Senior Legal Journalist & Contributing Editor Irvin 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 Evidence That Baby Powder Causes Ovarian Cancer Should Be Admissible At Trial: Report January 22, 2026 Trial Underway for Another Talcum Powder Cancer Lawsuit in California January 12, 2026 $1.5B Talcum Powder Verdict Returned by Baltimore Jury, In Latest Blow to J&J December 23, 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 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 Bard Port Catheter Fracture Caused Fragment Migration to Pulmonary Artery, Case Report Finds (Posted: today) A newly published case report describes a rare Bard port catheter fracture that occurred just six months after implantation, allowing a broken fragment to migrate into a patient’s pulmonary artery and requiring an additional medical procedure for removal. 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Evidence That Baby Powder Causes Ovarian Cancer Should Be Admissible At Trial: Report January 22, 2026
Bard Port Catheter Fracture Caused Fragment Migration to Pulmonary Artery, Case Report Finds (Posted: today) A newly published case report describes a rare Bard port catheter fracture that occurred just six months after implantation, allowing a broken fragment to migrate into a patient’s pulmonary artery and requiring an additional medical procedure for removal. MORE ABOUT: BARD POWERPORT LAWSUITBard PowerPort Settlement Talks May Heat Up as First Bellwether Trials Approach in 2026 (01/27/2026)Bard PowerPort Infection Lawsuit Set for Trial To Begin April 21, 2026 (01/15/2026)Cook Flexor Sheath Lawsuit Claims Defective Catheter Device Led to Woman’s Death (01/06/2026)
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