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.
Toyota and Lexus Fuel Pump Problems May Cause Engine Stalls, Accident Risk: Recall March 6, 2020 Russell Maas Add Your CommentsFederal highway safety officials have announced an expansion for a recall first issued in January, which now includes nearly 2 million Toyota and Lexus vehicles that may be equipped with fuel pumps that can fail unexpectedly, increasing the risk of a sudden engine stall and loss of vehicle control.The U.S. National Highway Traffic Safety Administration (NHTSA) posted the Toyota and Lexus recall expansion on March 4, after the Japanese auto maker recognized that additional vehicles may be prone to experience the same fuel pump problems that impacted several hundred thousand vehicles identified earlier this year.Toyota initially announced the fuel pump recall on January 15, impacting vehicles equipped with certain components manufactured by supplier, Denso Corporation of Japan. The pumps may cause the engine to stall without any advanced notice, and may fail to restart.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 COMPENSATIONIn cases of fuel pump failure these vehicles will enter a fail-safe mode, resulting in illumination of warning lights and reduced motive power. Unexpected full loss of power and the inability to restart the vehicle after a stall event are possible adverse outcomes, according to NHTSA investigators.The original recall impacted approximately 696,000 vehicles from the 2018 and 2019 model years, including Lexus LS 500, LC 500, RC 350, RC 300, GS 350, IS 300, ES 350, LX 570, GX 460 and RX 350 models, as well as certain Toyota 4Runner, Camry, Highlander, Land Cruiser, Sequoia, Sienna, Tacoma, and Tundra models. Some 2019 models of the Avalon and Corolla were also affected.After further investigation, now Toyota indicates that an additional 1,122,428 vehicles were equipped with a similar style of fuel pump, which may also face a higher rate of failure.The recall expansion includes certain 2014 through 2015 Toyota 4Runner and Land Cruiser, 2018 Avalon, Corolla, 2014 FJ Cruiser, 2017 Sienna and Lexus 2018 ES 350, 2018 through 2019 GS 300, 2013 and 2014 GS350, 2014 through 2015 GX 460, IS 350 and LX 570, 2014 IS F, 2018 through 2019 IS 350, LC 500H and LS 500H, 2013 through 2015 LS 460, 2015 NX 200T and RC350, 2017 RC 200T and RX 350 models.In total, there are now approximately 1,817,969 vehicles are impacted by both recalls.Toyota issued an interim notice to the original recall owners on February 17, 2020 and plans to send a second notice to the newly recalled vehicle owners by March 13, 2020 informing them of the defect.To date, replacement parts are currently not available, however the manufacturers indicate they will provide instructions in a third notice on May 3, 2020 with how to schedule an appointment at their local dealer to have the fuel pump replaced when they become available.Toyota is advising customers to be alert for warning lights and messages on the dashboard instrument panel or signs the engine is running rough or abnormal, as these could be indicators the fuel pump is experiencing the defect.Customers with additional questions are encouraged to contact Toyota Customer Experience Center at 1-800-331-4331 or the Lexus Guest Experience Center at 1-800-255-3987. 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, Lexus, Toyota 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 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 Walt July 13, 2021 Our 2019 Lexus 350 bought about 5 months ago at Arrowhead Lexus, Phoenix. Just had its second meltdown with warning lights flashing and stalled. We had this problem before and Lexus suggested we change our driving habits as stalling and loss of power is common in these vehicles. Fortunately I was not on the interstate as I probably would have been killed with my car being dead and others whizzing past me at 75 MPH. Thus far, Lexus said the vehicle was recalled and the fuel pump replaced but failed to notify us of this fact when we purchased the vehicle. Apparently the problem still exists. Iโm thinking they sold us a lemon. NameThis 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: yesterday)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: 2 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: 3 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)
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