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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
Baby Powder Asbestos Testing and Preservation Procedures Outlined by MDL Court November 6, 2019 Irvin Jackson Add Your CommentsA Special Master appointed by the U.S. District Judge presiding over all federal talcum powder lawsuits has established procedures and guidelines for testing samples of recalled Johnson’s Baby Powder, which was recently pulled from store shelves after the FDA found asbestos during routine testing.Johnson & Johnson currently faces more than 13,000ย Baby Powder lawsuitsย andย Shower-to-Shower lawsuits brought by women nationwide, involving claims that the manufacturer failed to warn that asbestos particles and talc contained in the widely used products may increase the risk of ovarian cancer, mesothelioma and other injuries.While the manufacturer has maintained that their talc-based powders are safe and do not contain asbestos, the manufacturer was forced to issue a Baby Powder recall last month, impacting 33,000 bottles, after the FDA found evidence of asbestos in a sample tested.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 COMPENSATIONIn a letter (PDF) sent to the parties in the federal litigation on November 1, Special Master Joel Pisano approved a supplemental order regarding the procedures for testing Johnson’s Baby Powder samples from the recalled lots, and outlined how the talcum powder samples should be preserved.Pisano is a retired federal judge, who was appointed to serve as a Special Master in the federal talcum powder litigation by U.S. District Judge Freda L. Wolfson, who is presiding over coordinated pretrial proceedings in the District of New JerseyThe order indicates that Johnson & Johnson has identified samples of milled talc related to the recalled Baby Powder, and shall notify plaintiffs if the company determines that testing in connection with the recent recall would deplete any sample, such that additional material would not be available to plaintiffs for independent testing. The order also outlines the procedure for preserving samples maintained by the company, as well as any bottles of recalled Baby Powder returned by consumers.The parties have been directed to meet and discuss whether returned samples will be divided for testing, and if so, an appropriate protocol for selecting such samples, with Pisano indicating that any disputes should be raised with the Court.Talcum Powder RecallThe Johnsonโs Baby Powder recall, announced on October 18, is expected to have a big impact on the pending litigation. Not only is it the first time Johnsonโs Baby Powder has ever been recalled, according to the manufacturer, but it also appears to verify assertions long made by critics about the risks associated with the company’s talc-based powder.The fact that the asbestos was discovered by an FDA test conducted by a scientist paid by Johnson & Johnson to serve as an expert witness in previous cases is expected to strengthen the plaintiffsโ position.Johnson & Johnson has indicated that its own independent testing has found no trace of asbestos, but FDA officials have continued to stand by the agency’s findings and plaintiffs have not been provided an opportunity to test the recall samples.In addition to the civil lawsuits, the manufacturer also faces aย criminal probe into what it knew about asbestos being in its talcum powder products and when it knew it. Some internal documents revealed during the litigation and media investigations suggestย Johnson & Johnson may have known about the potential presence of asbestosย in its products since the 1950s, but failed to warn regulators or consumers.Exposure to asbestosย fibers has been linked to a number of forms of respiratory illnesses and cancer, such as mesothelioma, lung cancer, and asbestosis.Mesothelioma is a rare form of cancer, where the only known cause is asbestos exposure. As a result of a long latency period of between 20 and 40 years between exposure to asbestos and diagnosis, the cancer is often at a very advanced stage by the time it is discovered and usually results in death.Unless Johnson & Johnson is able to exclude plaintiffs’ expert witnesses from testifying in the federal litigation, it is expected that Judge Wolfson will schedule a series of bellwether trials to gauge how juries may respond to certain evidence that is likely to be repeated throughout the cases. 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, Baby Powder Recall, Johnson & Johnson, Mesothelioma, Ovarian Cancer, Talc, Talcum PowderMore Talcum Powder Lawsuit Stories J&J Agrees to $5.5B Talcum Powder Settlement Payout to Resolve Ovarian Cancer Lawsuits July 29, 2026 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 0 Comments URLThis 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 DraftKings Predictions ‘Event Contracts’ Are Unlicensed Sports Betting (Posted: today)A California man has filed a class action lawsuit alleging DraftKings offers sports betting through its Predictions platform in states where it lacks sportsbook authorization.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITFanDuel Addiction Lawsuit Alleges Targeted Advertising Caused Substantial Gambling Losses (08/19/2026)DraftKings Predictions Lawsuit Seeks Refunds for Illegal Sports Betting Losses (08/11/2026)Class Action Lawsuit Claims DraftKings Is Dodging State Gambling Laws (07/31/2026) Judge Appoints Spinal Cord Stimulator Lawyers to Leadership Roles in Boston Scientific MDL (Posted: yesterday)A federal judge has appointed a group of plaintiffs attorneys to leadership positions in the growing Boston Scientific spinal cord stimulator federal litigation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuit Alleges Spine Implant Caused Nerve Damage, Shocks (08/18/2026)Nevro Stimulator Lawsuit MDL Request Opposed by Manufacturer (08/14/2026)Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (08/10/2026) Similac Settlement Provides $670M Payout To Resolve 2,000 NEC Lawsuits (Posted: 4 days ago)Abbott Laboratories has agreed to pay $670 million to resolve more than 2,000 Similac NEC injury lawsuits, as the first federal NEC trial against competitor Mead Johnson gets underway.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITMissouri Appeals Court Orders New Trial for Similac, Enfamil NEC Lawsuit (08/20/2026)Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week (08/11/2026)Neocate Infant Formula Lawsuit Alleges Nutritional Defect Caused Rickets, Bone Fractures (08/05/2026)
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