Lyft Driver Assault Lawsuit Claims Rideshare Service Performs Inadequate Background Checks Despite Similar Attacks
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.
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.
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.
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.
Volkswagen Recall Issued Over Failure to Warn When Key Is In Ignition, Creating Crash Risk December 11, 2018 Russell Maas Add Your CommentsNearly 74,000 Volkswagen vehicles have been recalled, due to concerns that a defect may prevent the driver from receiving an alert when the key is still in the ignition, which may increase the risk of roll away problems, accidents and stolen vehicles.ย The U.S. National Highway Traffic Safety Administration (NHTSA) announced the Volkswagen recall this month, indicating that certain models may not comply with Federal Motor Vehicle Safety Standards (FMVSS) that require alerts if the key is in the ignition when the door is open.Under FMVSS number 14, automobile manufacturers must equip vehicles with an audible warning if the driverโs door is left open while the key is still in the ignition. The failure to alert drivers could increase the risk of theft, and could also increase the risk of a crash and injury to any occupants left inside the vehicle.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 affects 2018 through 2019ย Volkswagen Atlas models manufactured from December 22, 2016 through November 10, 2018; 2019 Volkswagen Jetta models manufactured from October 11, 2017 through November 8, 2018; and 2018 through 2019 Volkswagen Tiguan models manufactured from March 1, 2017 through November 8, 2018.According to Volkswagen, 10,109 Atlas models, 37,992 Jetta sedans, and 25,444 Tiguan crossovers are included in the recall, totaling 73,545 vehicles.An investigation opened by Volkswagen and NHTSA found a manufacturing defect in which the data container was not properly coded, and could fail to sound an audible chime when the key is left in the ignition.Volkswagen Group of America, Inc. announced they will begin notifying owners of the recall and will provide instructions on how to schedule a free repair appointments at their local dealer, where dealers will reprogram the instrument cluster.The recall is anticipated to begin on January 18, 2019. Customers with additional questions or concerns may contact Volkswagen customer service at 1-800-893-5298 and reference the recall campaign number 90L3 and 90L4. 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: Auto Accident, Auto Recall, Volkswagen Image Credit: Image via <a href="http://www.shutterstock.com/gallery-365671p1.html?cr=00&pl=edit-00">FotograFFF</a> / <a href="http://www.shutterstock.com/editorial?cr=00&pl=edit-00">Shutterstock.com</a>More Lawsuit Stories Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit April 22, 2026 Lyft Driver Assault Lawsuit Claims Rideshare Service Performs Inadequate Background Checks Despite Similar Attacks April 22, 2026 Lawsuit Alleges Unsafe Conditions at Planet Fitness Gym Resulted in Womanโs Injuries April 22, 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 Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: today)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026) Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: yesterday)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026) SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 2 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)
Lyft Driver Assault Lawsuit Claims Rideshare Service Performs Inadequate Background Checks Despite Similar Attacks April 22, 2026
Lawsuit Alleges Unsafe Conditions at Planet Fitness Gym Resulted in Womanโs Injuries April 22, 2026
Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (Posted: today)A Depo-Provera meningioma lawsuit argues that Pfizer had a duty to warn women about scientific evidence linking the birth control shot to potential brain tumor growth yet failed to do so.MORE ABOUT: DEPO-PROVERA LAWSUITHearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)Depo-Provera Meningioma Lawyers Reappointed to MDL Leadership Roles (03/25/2026)
Judges Will Consider MDL for Dupixent Cancer Lawsuits Late Next Month (Posted: yesterday)A group of federal judges will determine whether all Dupixent cancer lawsuits should be formed into a multidistrict litigation, following oral arguments set for May 28.MORE ABOUT: DUPIXENT LAWSUITDupixent Injections Caused Peripheral T-Cell Lymphoma (PTCL) Diagnosis: Lawsuit (04/06/2026)Link Between Dupixent and CTCL Withheld From Users, Medical Community: Lawsuit (03/31/2026)Drug Makers Agree Dupixent Cancer Lawsuits Should Be Centralized in MDL (03/26/2026)
SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (Posted: 2 days ago)A product liability lawsuit alleges unlicensed Abbott representatives made real-time spinal cord stimulator programming decisions based on a Texas womanโs responses, improperly modifying the device and contributing to her injuries.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITWaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)Boston Scientific Neuromodulation Lawsuit Claims Spinal Cord Stimulator Exacerbated Chronic Pain (04/08/2026)Medtronic SCS Lawsuit Alleges Intellis LT Neurostimulator Caused Worsening Pain (04/03/2026)