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.
Volkswagen, Audi Recall Issued Over Brake System Problems January 10, 2017 Russell Maas Add Your CommentsMore than 130,000 Audi and Volkswagen vehicles have been recalled due to problems with the Antilock Brake System (ABS) control unit, which may fail and increase the risk of an auto accident.ย The Volkswagen recall was announced by the U.S. National Highway Traffic Safety Administration (NHTSA) on January 6, following dozens of consumer reports of the ABS or Electronic Stability Control (ESC) failing while attempting to stop the vehicle. To date, no injuries or crashes have been reported in relation to the recall.The recalled Audi and VW vehicles are equipped with both ABS control units and ESC activation features to stabilize the vehicle as the brakes are applied. Volkswagen has determined that an incorrect solder compound used during the manufacturing process may cause the ground solder to prematurely crack due to thermo-mechanical stress, ultimately leading to insufficient power supply to the braking systems.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 COMPENSATIONIf this problem occurs, the brake system warnings will light up on the dashboard and the vehicle’s braking system stabilizing functions may fail, making it hard to control the vehicle when the brakes are applied.Owners are being urged to contact dealers immediately if these icons illuminate to avoid potential loss of control situations and increased crash hazards.The recall affects an estimated 135,683 model year 2009-2010 Volkswagen Jetta A5 Sedans, 2009 Volkswagen Jetta SportWagens, Eos, GTI, Rabbit and Audi A3 vehicles, and 2010 Volkswagen Golf A6 vehicles.Volkswagen Group of America Inc. announced it will notify owners of the potential defect and provide instructions on how to schedule a free repair at their local dealer, who will update the ABS control module software to improve the moduleโs self-testing abilities. Any module that fails the new diagnostic testing will be replaced free of charge by Volkswagen.Customers with further question are being asked to contact Volkswagen’s customer service at 1-800-893-5298. Owners may also contact the NHTSA Vehicle Safety Hotline at 1-888-327-4236 to report adverse events and vehicle related defects. 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: Audi, 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 AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis August 7, 2026 Lawsuit Alleges SteriCare Solution Caused Sepsis, Wrongful Death August 7, 2026 AirTag Lawsuit Claims Apple Tracking Devices Used to Stalk Woman August 7, 2026 7 Comments Gi December 10, 2021 Will someone tell me what my recourse is? I had this intermittent brake light problem come on occasionally, and then more persistent until it finally set off the, “J104 ABS Control Module” check engine light. The service advisor at my local VW dealer approached me with a mouth full of food and began to spit out a dozen reasons why they cannot fix my ABS. Specifically, he said it was broken and they only reprogram working modules. I read the reason for the recall is faulty ground solder, so how could the ABS not fail? Any help would be greatly appreciated! Best Regards, G… Hamza January 21, 2021 I have the same issue. And i had an accident be cause of this one. I even have a video thay shows me driving with 140km/h and after a hard brake. The red light shows and my car spin in 180 degree. And the car flips. I was with my brother and we got some injury. I still have the issue until now. The issue is still reproducible. Now am driving my car slowly.. can some one help. Am in morocco and i bought the car from germany. Daryl November 7, 2019 Having same problem with the ABS module on my 09 Jetta. Had no issue with it, received a recall notice for an update to supposedly fix problem. Did it being pro active then all the sudden I have brake problems. Dealers says they won’t warranty cause of a code it doen’t pull. I call BS. think something fishy going on. ALLYSON November 12, 2018 We are having the same problem with our 2009 VW Rabbit with only 78,683 miles and feel helpless because VW won’t replace the ABS module because it doesn’t show a certain code and it’s almost a $2000.00 fix. I wish I knew if there was any type of legal action we could take? Hugo March 9, 2018 I’m going through the same issue with an ’09 GTI that is included in the recall for ABS module. If it is defective regardless as to whether they are getting the correct codes or not it should be replaced. Has anyone had any luck getting VW to cover the repair? Barry March 3, 2017 My ’09 VW GTI is included in the latest recall for the ABS module. As far as history, my ABS brakes went out about 1 year ago and they said I needed a new module, which I didn’t get fixed when considering they were asking $2400 to fix it. Now that there is a recall, I took it in and they said they would NOT replace the module under the recall (something about not having the correct computer codes) but they still confirm that the ABS module is broken and needs to be replaced. Being really confused now, IS THERE ANY ADDITIONAL RECOURSE THAT I CAN TAKE UP AGAINST VW, to replace my ABS. Sterling February 7, 2017 I had my abs fail in my 2009 audi a3 Quattro and caused me to crash into the woods with zero control of brakes or throttle response, airbags didn’t deploy either but audi engineers looked over the car and said it functioned as Designed? I don’t think this is right. The abs and traction lights have come on in the past a few times but always went out after turning the vehicle off and back On? I only owned the car since November to replace my bought back jetta tdi and didn’t expect more issues , especially as dangerous as this! 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 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)
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)