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.
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
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.
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.
Exposure To Asbestos In Talc Products Can Cause Mesothelioma: Study March 19, 2020 Irvin Jackson Add Your CommentsThe findings of a new study appear to confirm concerns about the health risks from asebstos in talcum powder, indicating that traces of the toxic fibers found in some cosmetic talc-based products may cause a fatal form of lung cancer known as mesothelioma, which is only known to result from asbestos exposure.Researchers from Peninsula Pathology Associates in Virginia published a study this week in the American Journal of Industrial Medicine, which warns that mesothelioma can develop following exposure to anthophyllite and tremolite asbestos contaminants in cosmetic talcum powder. The findings come just days after federal regulators reported that they found multiple instances of asbestos contamination in talcum powder products last year.Mesothelioma is a rare and deadly form of cancer, which is only known to occur as a result of exposure to asbestos particles. In many cases, the cancer has developed among individuals exposed to asbestos decades ago, or among family members of workers in certain industries, where the fibers were carried home on their clothes or in their hair.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 this latest study, researchers looked at data on 75 individuals, including 64 women and 11 men, who developed malignant mesothelioma. For all of the subjects, their only known exposure to asbestos was through the repeated use of cosmetic talcum powders. The researchers were able to exam 11 of the patients for asbestiform fibers.Of the 75 subjects, the mean age at diagnosis was 61. Most had been exposed for about 33 years. In 12 cases, the individuals were less than 45 years old.Researchers were able to find asbestiform fibers in all 11 subjects they were able to medically exam. All 11 showed the presence of either anthophyllite and/or tremolite asbestos.โMesotheliomas can develop following exposures to cosmetic talcum powders,โ the researchers concluded. โThese appear to be attributable to the presence of anthophyllite and tremolite contaminants in cosmetic talcum powder.โThe FDA has been testing cosmetic talcum powder products throughout 2019, and continues to do so. On March 9, the agency released the findings from its 2019 investigation, revealing that out of 43 samples from cosmetic products tested, nine were positive for asbestos.However, the FDA indicates that no new talc asbestos contamination announcements are being made at this time, as those announcements were issued as soon as the samples were tested. This included recalls of Claireโs cosmetics products in March 2019, as well as a very high profileย Johnson & Johnson Baby Powder recallย issued in October.Much of the attention to date has been on the alleged presence of asbestos in Johnson & Johnson talcum powder products.Johnson & Johnson currently faces about 18,000ย Baby Powder lawsuitsย andย Shower-to-Shower lawsuitsย pending in courts nationwide, each raising similar claims the manufacturer has known for decades their products may contain asbestos and increase the risk of cancer, yet failed to warn consumers.While most of the claims involve women diagnosed with ovarian cancer following years of talcum powder use, a smaller number involve individuals diagnosed with mesothelioma, which is a rare and particularly deadly form of cancer that is only known to occur as aย result of asbestos exposure.The company also currently faces aย criminal probe into what it knew about asbestos being in its talcum powder productsย and when it knew of the risk.Most of the U.S. litigation is currently pending in the federal court system, where a U.S. District Judge is currently evaluating 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 under the federalย Daubertย standard, it is expected that a series of โbellwetherโ cases will be scheduled for trial, which will increase pressure on the manufacturer to consider negotiating more wide-scaleย talcum powder cancer settlementsย to avoid thousands of individual cases going before juries. 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, Cosmetics, Johnson & Johnson, Mesothelioma, Shower to Shower, 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 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: today)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026) Lawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (Posted: yesterday)An Alabama woman has filed a lawsuit alleging a Boston Scientific spinal cord stimulator failed to relieve her chronic pain, instead causing complications that ultimately required surgery to remove the entire system.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITSpine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026)Abbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026) Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 2 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)
AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: today)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
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Covidien Hernia Mesh Lawsuit Payout of $88M Awarded in First MDL Bellwether Trial (Posted: 2 days ago)The first Covidien hernia mesh bellwether trial has ended in an $88 million verdict for the plaintiff, who suffered bowel resectioning and revision surgery after his Symbotex hernia mesh failed.MORE ABOUT: HERNIA MESH LAWSUITHernia Mesh Failure Lawsuit Alleges ProGrip Implant Was Prone to Breaking and Fragmenting (08/03/2026)Bard Composix Kugel Hernia Mesh Lawsuit Claims Defective Implant Required Bowel Resection (07/27/2026)First Covidien Hernia Mesh Lawsuit Trial Over Symbotex Problems To Begin Next Week (07/10/2026)