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 Tiguan Recall Due to Risk of Fire from Sunroof Lightbar August 14, 2018 Russell Maas Add Your CommentsMore than 45,000 Volkswagen SUVโs have been recalled due to a risk that an ambient light bar in the the sunroof may short circuit and overheat, posing a risk of vehicle fires.ย A Volkswagen Tiguan recall was announced by the U.S. National Highway Traffic Safety Administration (NHTSA) on August 7, following at least two consumer reports that suggest the LED module on the sunroof ambient light bar short circuited, causing smoke and a burning smell to fill the vehicles.The recall involves certain Tiguan vehicles that are equipped with panoramic sunroofs with ambient light bars that have the potential to short circuit when exposed to high humidity. To date, no injuries or fires have been reported in relation to the recall.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 COMPENSATIONAn estimated 45,457 Volkswagen Tiguan SUVs from the 2018 model year have been recalled, which were manufactured from December 2016 through July 2018 and distributed throughout the United States to licensed dealers.The NHTSA is advising consumers to stop using the sunroof features and if the smell of burning or smoke is noticed inside the cab, consumers should stop using the vehicles and contact their local dealer immediately.Volkswagen stated the recall is expected to begin on September 11, and will be sending written notice to all customers with instruction on how to schedule a free inspection at their local dealer.Dealers will be instructed to disconnect the LED light module from its power supply and apply aluminum tape. The LED lights will no longer be functional after this repair, and a subsequent service campaign will be launched by Volkswagen when a safe resolution and parts are available.Customers with additional questions or concerns regarding the recall may contact Volkswagen customers service at 1-800-893-5298 and reference the recall campaign number 60D1. 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 Recall, Car Fire, 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 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims April 16, 2026 HeartMate II Wrongful Death Lawsuit Claims LVAD Implant Caused Thrombosis April 16, 2026 Video Game Addiction Lawsuit Claims Devs Use Behavioral Manipulation on Kids April 16, 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 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 Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: today)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026) Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: yesterday)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-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)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026) WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 2 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston 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)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)
Jury Selection Underway in First Bard PowerPort Trial Over Infection Claims (Posted: today)The first Bard PowerPort lawsuit bellwether trial commences next week involving claims that a man suffered a severe infection due to the port catheter’s allegedly defective design.MORE ABOUT: BARD POWERPORT LAWSUITJudge Blocks Juries From Hearing About IVC Filter Problems in Bard PowerPort Trials (04/08/2026)Port-a-Cath Lawsuit Alleges Power P.A.C. Break Down Resulted in Serious Port Catheter Infection (03/31/2026)Final Pretrial Conference in Bard PowerPort Lawsuit To Be Held April 9 (03/27/2026)
Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (Posted: yesterday)A federal judge has scheduled general causation hearings for Depo-Provera brain tumor lawsuits for June 24 through 26.MORE ABOUT: DEPO-PROVERA LAWSUITHigh-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)Depo-Provera Brain Tumor Symptoms Reported Among Birth Control Users (03/19/2026)
WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (Posted: 2 days ago)A Louisiana man’s Boston Scientific WaveWriter Alpha SCS lawsuit claims the implant failed to provide the promised pain relief and, in fact, made things worse before it needed to be surgically removed.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston 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)Nevro Spinal Cord Stimulator Lawsuits Filed Over Device Malfunction, Failure (03/30/2026)