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.
Aqua Lung Diving Vest Recall Issued Due to Drowning Risk March 22, 2013 Russell Maas Add Your CommentsAbout 110,000 diver’s buoyancy compensators have been recalled due to a potential risk that the handles may tear from the vest and disable the diver from removing weighted pockets that are used to rise to the surface in emergency situations. ย An Aqua Lung Buoyancy Compensator recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on March 21, after Aqua Lung received at least 236 reports of the handles detaching from the weighted pockets.The vest are equipped with rubber handles on the pockets that have weights in them to allow the diver to descend easily. The hazard stems from the rubber handles ripping, preventing the diver from removing the weights, which can pose an increased drowning hazard when the diver needs to surface. However, to date, no reports of injury or drowning have been reported in connection with the defect.Do You Know about…Spinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONDo You Know AboutโฆSpinal Cord Stimulator lawsuitsSpinal cord stimulator lawsuits are being investigated for individuals who suffered unnecessary shocks, burns or other problems, often resulting in the need for additional surgery to remove the SCS.Learn MoreSEE IF YOU QUALIFY FOR COMPENSATIONThe recall includes all of the following Aqua Lung buoyancy compensators with SureLock II rubber handles attached to the weight pockets; Axiom, Axiom i3, Balance, Black Diamond, Dimension, Libra, Lotus, Pearl, Pearl i3, Pro LT, Pro QD, Pro QDi3 and Zuma buoyancy compensators.The recalled models measure 2 inches tall by 4 inches wide and have gray rubber handles with “SureLock” molded into the pocket and the model name printed on the inside of the back pad or the pocket’s right lobe.The buoyancy compensators were manufactured in China and Mexico and imported by Aqua Lung America, of Vista, California, where they were sold at various sporting goods and scuba diving stores nationwide from September 2008 through September 2012 for between $460 and $700.The CPSC recommends that consumers stop using the recalled buoyancy packs immediately and contact Aqua Lung at (855) 355-7170 or return the two weighted pockets to an authorized Aqua Lung dealer to receive a free replacement and inspection. Consumers may also visit Aqua Lung online at aqualung.com and navigate to the “Recall Notice” for further inquiry. Written by: Russell MaasManaging Editor & Senior Legal JournalistRussell Maas is a paralegal and the Managing Editor of AboutLawsuits.com, where he has reported on mass tort litigation, medical recalls, and consumer safety issues since 2010. He brings legal experience from one of the nationโs leading personal injury law firms and oversees the siteโs editorial strategy, including SEO and content development. Tags: Drowning Image Credit: |More Lawsuit Stories J&J Agrees to $5.5B Talcum Powder Settlement Payout to Resolve Ovarian Cancer Lawsuits July 29, 2026 CTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use July 29, 2026 Instant Pot Duo Nova Lawsuit Alleges Defective Pressure Cooker Caused Serious Burns July 29, 2026 0 Comments PhoneThis 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 J&J Agrees to $5.5B Talcum Powder Settlement Payout to Resolve Ovarian Cancer Lawsuits (Posted: today)A $5.5 billion settlement deal could resolve nearly 80,000 talcum powder cancer lawsuits that claim Johnson & Johnson products were contaminated with asbestos.MORE ABOUT: TALCUM POWDER CANCER LAWSUITSAdditional Talks To Settle Talcum Powder Cancer Lawsuits Set for April 13 (03/20/2026)Ovarian Cancer Talcum Powder Lawsuit Results in $250K Verdict Against J&J (02/16/2026)Evidence That Baby Powder Causes Ovarian Cancer Should Be Admissible At Trial: Report (01/22/2026) Chlorpyrifos Exposure Lawsuit Claims Pesticide Caused Farmer’s Parkinson’s Disease Diagnosis (Posted: yesterday)A chlorpyrifos lawsuit claims years of exposure through residence and work left a California man with a Parkinson’s disease diagnosis.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITChlorpyrifos Parkinsonโs Disease Lawsuit Claims Years of Insecticide Exposure Caused Neurological Side Effects (07/22/2026)Chlorpyrifos (CPF) Exposure Linked to Abnormal Brain Development in Children: Study (08/27/2025)Court Ruling Allows EPA to Proceed with Chlorpyrifos Ban (10/23/2023) Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (Posted: 2 days ago)Abbott faces a Proclaim spinal cord stimulator lawsuit by a man who says the device not only failed, but that he was repeatedly electrocuted when sales representatives without medical licenses tried to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)Boston Scientific Spinal Cord Stimulator Lawyers to Meet With MDL Judge for Initial Conference Aug. 5 (07/16/2026)Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (07/13/2026)
J&J Agrees to $5.5B Talcum Powder Settlement Payout to Resolve Ovarian Cancer Lawsuits (Posted: today)A $5.5 billion settlement deal could resolve nearly 80,000 talcum powder cancer lawsuits that claim Johnson & Johnson products were contaminated with asbestos.MORE ABOUT: TALCUM POWDER CANCER LAWSUITSAdditional Talks To Settle Talcum Powder Cancer Lawsuits Set for April 13 (03/20/2026)Ovarian Cancer Talcum Powder Lawsuit Results in $250K Verdict Against J&J (02/16/2026)Evidence That Baby Powder Causes Ovarian Cancer Should Be Admissible At Trial: Report (01/22/2026)
Chlorpyrifos Exposure Lawsuit Claims Pesticide Caused Farmer’s Parkinson’s Disease Diagnosis (Posted: yesterday)A chlorpyrifos lawsuit claims years of exposure through residence and work left a California man with a Parkinson’s disease diagnosis.MORE ABOUT: CHLORPYRIFOS PARKINSONโS DISEASE LAWSUITChlorpyrifos Parkinsonโs Disease Lawsuit Claims Years of Insecticide Exposure Caused Neurological Side Effects (07/22/2026)Chlorpyrifos (CPF) Exposure Linked to Abnormal Brain Development in Children: Study (08/27/2025)Court Ruling Allows EPA to Proceed with Chlorpyrifos Ban (10/23/2023)
Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (Posted: 2 days ago)Abbott faces a Proclaim spinal cord stimulator lawsuit by a man who says the device not only failed, but that he was repeatedly electrocuted when sales representatives without medical licenses tried to reprogram it.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Faces Spine Stimulator Lawsuit Brought Jointly by 17 Injured Patients (07/23/2026)Boston Scientific Spinal Cord Stimulator Lawyers to Meet With MDL Judge for Initial Conference Aug. 5 (07/16/2026)Spinal Cord Stimulator Lawsuit Claims Boston Scientific Sales Reps Made Unauthorized Device Adjustments (07/13/2026)