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.
Subaru Brake Light Problems Lead To Recall of 1.3 Million Vehicles March 13, 2019 Russell Maas Add Your Comments More than a million Subaru Forrester, Impreza and other vehicles have been recalled, following nearly a dozen reports of a brake light switch failing, which may prevent the rear lights from illuminating and not allow the vehicle to be shifted out of the Park position. The Subaru brake light recall was announced by the U.S. National Highway Traffic Safety Administration (NHTSA) this month, after the auto maker determined that contaminants can enter the brake light switch and prevent it from illuminating, which creates an increased accident risk. The recalled Subaru vehicles are all equipped with an electronic brake switch, which may become exposed to silicone gas. In this event, silicone dioxide may form a layer on the switch contact terminal and cause a connectivity failure. Do You Know about… SPORTS BETTING ADDICTION LAWSUITs Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. Learn More SEE IF YOU QUALIFY FOR COMPENSATION Do You Know Aboutโฆ SPORTS BETTING ADDICTION LAWSUITs Gambling addiction and severe financial losses have been linked to popular sports betting platforms like DraftKings, FanDuel, and Caesars. Lawsuits are being filed by young adults and students who were targeted by deceptive promotions, addictive app features, and aggressive marketing tactics. Learn More SEE IF YOU QUALIFY FOR COMPENSATION In the event of the contact failure, Subaru warns the brake lights may malfunction and not illuminate when the brake is pressed, increasing the odds of a rear end collision. In addition, the break light problem may cause the keyless ignitions to fail to start, and the variable transmission may not be allowed to shift out of the Park position. Affected vehicles equipped with anti-lock brakes, vehicle dynamic controls and lane-departure systems may also fail to alert and assist drivers in avoiding an imminent crash. The recall affects approximately 526,941 model year 2014 through 2016 Foresters, 363,566 model year 2013 through 2017 Crosstrek vehicles, and 413,000 model year 2008 through 2016 Impreza and WRX models. Subaru announced it will be withdrawing approximately one million more impacted vehicles from the Japanese market, bringing the total of recalled vehicles globally to 2.3 million. The manufacturer will begin notifying customers of the recall late next month and will provide instructions on how to schedule a repair appointment at their local dealer, where dealers will be instructed to replace the brake light switch free of charge. The recall is expected to begin on April 29, 2019. Customers with additional questions or concerns regarding their vehicle should contact Subaru customer service at 1-844-373-6614. Written by: Russell Maas Managing Editor & Senior Legal Journalist Russell 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: Auto Accident, Auto Recall, Subaru, Subaru Forester More Lawsuit Stories Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week March 12, 2026 Enfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects March 12, 2026 Stainless Steel Apple Watch Bandโ Lawsuit Filed Over Burn Injury Risks March 12, 2026 0 Comments X/TwitterThis 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 Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: today) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026) Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: yesterday) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026) Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: 2 days ago) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)
Enfamil Lawsuit Claims Premature Infant Required Partial Intestine Removal From NEC Side Effects March 12, 2026
Lawyers To Nominate Hair Relaxer Cancer Cases for Early Bellwether Trials Next Week (Posted: today) Plaintiffs and defendants involved in hair relaxer cancer lawsuits are expected to turn in a list of 12 cases that the parties believe are fit to serve as bellwether trials. MORE ABOUT: HAIR RELAXER LAWSUITCourt Outlines Procedures When Women Die After Filing a Hair Relaxer Cancer Lawsuit (02/25/2026)Hair Extension Chemicals May Be More Harmful Than Previously Thought: Study (02/17/2026)MDL Judge Issues New Deadlines for Hair Relaxer Lawsuit Bellwether Trial Preparations (02/04/2026)
Cartiva Implant Recall Lawsuits Move Forward, as Plaintiffs Seek Compensation for Big Toe Surgery Failures (Posted: yesterday) Cartiva implant lawsuits are moving forward in federal court as patients across the United States seek compensation for complications linked to the recalled big toe device. MORE ABOUT: CARTIVA IMPLANT LAWSUITCartiva Synthetic Cartilage Implant Lawsuits Centralized in Federal MDL (02/10/2026)Lawsuit Alleges Cartiva Implant Loosened, Degraded in Great Toe (02/05/2026)Big Toe Fusion Lawsuit Filed Over Failed Cartiva SCI Implant (01/27/2026)
Abbott Spinal Cord Stimulator Lawsuit Alleges Defects Caused Lead Migration, Electric Shocks (Posted: 2 days ago) An Abbott spinal cord stimulator lawsuit filed by three women says the product was defectively designed, inappropriately approved by the FDA, and left them with severe injuries, worsening pain and the need for removal surgery. MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Claims Airport Body Scanner Destroyed Woman’s Spinal Cord Stimulator, Requiring Surgical Removal (03/03/2026)Medtronic Spinal Cord Stimulator Lawsuit Filed Over Unnecessary Shocking Sensations (02/27/2026)Boston Scientific Pacemaker Lawsuit Claims Recalled Device Caused Life-Threatening Situation (02/25/2026)