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.
Audi A3 Recall Issued Over Passenger Side Air Bags Which May Deactivate March 30, 2021 Russell Maas Add Your CommentsMore than 150,000 Audi A3 vehicles from recent model years are being recalled due to problems with a sensor that may fail and turn off the passenger side air bag when someone is occupying the seat.The U.S. National Highway Traffic Safety Administration (NHTSA) announced the Audi A3 recall on March 22, indicating the passenger occupant detection system (PODS) may malfunction and deactivate the front seat passenger airbag, increasing the risk of serious injury or death in the event of a crash.The manufacturer, Volkswagen, first became aware of the defect in early 2019, following several warranty claims indicating the “passenger airbag off” warning light on the instrument panel came on by itself while someone was in the seat.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 COMPENSATIONFollowing an internal investigation, the German automaker determined an electrical connector can malfunction and deactivate the front passenger-side airbag, and subsequently issued a recall for 138,000 model year 2015 through 2019 A3 cars in June 2019. However, following new reports of airbag problems with the previously recalled Audi A3 vehicles, even after the repair remedy was performed, Volkswagen determined an additional issue exists within the PODS system beyond the issue addressed by the 2019 recall.NHTSA officials warn that in the event of a automobile accident in which the airbag does not deploy, passengers could be at an increased risk of serious injury or death.While the root cause of the problem is still unknown, Volkswagen announced it is recalling 153,152 model year 2015 through 2020 Audi S3 Sedan, A3 Sedan, 2016 through 2018 A3 Etron, 2017 through 2020 RS3 Sedan, and 2015 through 2019 A3 Cabriolet vehicles due to the airbag problem.Volkswagen recommends occupants of recalled vehicles avoid using the front passenger seat while the investigation into the problem continues.The automaker announced it will begin notifying customers of the recall with an initial notice by May 21, and will provide a second notice when a remedy becomes available. Customers with additional questions or concerns surrounding the recall are encouraged to contact Audi customer service at 1-800-253-2834 and reference the recall campaign number 69BY. 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: Airbag, Audi, Auto Accident, Auto Recall, VolkswagenMore Lawsuit Stories Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect June 12, 2026 Xcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis June 12, 2026 Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026 1 Comments Carl September 1, 2022 I own a 2015 Audi A3 which has had a recall for over one year regarding the front passenger side airbag. I have contacted my local Audi dealer as well as Audiโs national hotline. My local dealers say parts to fix the issue are not available. The Audi National team has emailed me and advised the same thing. They also say that as long as the front passenger side airbag light does not come on it is ok for someone to sit in the front passenger seat. The light on my car has come on every time someone sits there. For over 1 year I have not been able to use this vehicle for the purpose which it was intended. Audi has offered NO OTHER solution or compensation for not be able to use my car. They have however sent me several offers to trade my defective car in on a new one. Make me wonder how they can do this when by law they cannot sell any vehicle which has a recall on it. I talked to both Audi USA today and my local Audi dealer and both advised that parts are still not available but neither offer any compensation or alternative 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 Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026) Suboxone Dental Erosion Lawsuit Alleges Indivior Should Have Known About Tooth Decay Risks (Posted: 3 days ago)A Suboxone dental erosion lawsuit filed by nine plaintiffs accuses the manufacturer of knowing the film strips caused severe tooth decay and other oral health problems, but failed to warn the medical community or patients.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITSuboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (05/20/2026)Lawsuit Alleges Suboxone Dental Damage Warnings Were Issued Too Late (05/07/2026)Study Finds No Birth Defect Risks From Suboxone When Compared to Methadone (04/30/2026) Covidien Mesh Lawsuit Cleared for Trial Over Hernia Repair Complications (Posted: 4 days ago)A Covidien hernia mesh lawsuit will go before a jury next month after a federal judge rejected the manufacturer’s motion to have the case dismissed.MORE ABOUT: HERNIA MESH LAWSUITBard Ventralight Lawsuit Claims Hernia Mesh Failure Resulted in Ongoing Physical Disabilities (06/03/2026)Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery (05/21/2026)Covidien ProGrip Mesh Complications Lawsuit Filed Over Alleged Defects and Failure To Warn Patients (04/21/2026)
Rezurock Lawsuit Claims GVHD Medication Caused Debilitating Skin Condition, Prurigo Nodularis June 12, 2026
Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (Posted: 2 days ago)A spinal cord stimulator lawsuit claims that the Abbott Proclaim XR 5 system failed to treat a manโs chronic pain, instead leaving him with shocks and burning sensations.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)Lawsuit Indicates Spinal Cord Stimulator Lead Complications Resulted in Shocks, Removal Surgery (06/02/2026)Spinal Cord Stimulator Malpractice Lawsuit Claims Device Left Veteran Partially Paralyzed (05/29/2026)
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