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.
Two Razor Recalls: Four-Wheel Electric Vehicles and Three-Wheel Scooters Recalled September 26, 2008 AboutLawsuits Add Your CommentsOn September 25, 2008, Razor USA LLC of Cerritos, California, and the U.S. Consumer Product Safety Commission (CPSC) announced a Razor electric vehicle recall and Razor scooter recall involving a combined total of around 133,000 vehicles.About 103,000 Razor PowerWing Three-Wheeled Scooters were recalled because of sharp edges on the underside of the foot platform, which could pose a risk of severe lacerations for children using the scooters.Razor has received 10 reports of injuries, and at least 4 people required surgery to repair their Achilles tendon which connects the calf muscle to the heel bone. A torn Achilles tendon is a serious injury which can result in a lengthy recovery after surgery and permanent residuals.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 Razor scooters were sold between October 2007 and September 2008 for about $100 each. They were manufactured in either black or silver, with small foot platforms that extend out from the center support bar in a wing-like fashion.The recalled Razor Power Wing Scooters contain product serial numbers starting with Y0708 to Y0712 and Y0801 to Y0808 on the bottom of the scooter near the front wheel. Products that contain an oval sticker next to the serial number with a โVโ followed by any letter e.g. VE, VF etc. are not part of this recall.A separate Razor recall was issued for about 30,000 of their Dirt Quad Electric Powered four-wheel vehicles. The small ride-on vehicles, which resemble an ATV, contain a defective module for the throttle which could cause it to suddenly surge forward. This could pose a serious risk of injury to the rider or bystanders.Razor has received at least 60 reports of problems involving the defective throttle, and at least 10 people have suffered a personal injury.The electric Razor Dirt Quad bikes were sold throughout the United States between August 2006 and September 2007 for about $400 each. They contain product identification numbers beginning with 1031 10-01 or 1031 10-02 located on the bar code that is fixed on the right step of the vehicle, on the charger and on the retail packaging. Product ID numbers that start with 1031 10-03 or later are not included in the recall.Consumers have been advised to immediately stop using the recalled Razor PowerWing scooters and Razor four wheel electric vehicles. Razor is offering replacements of the controller on the electric vehicle and replacements of the foot platforms for the scooters. Tags: Razor Scooter Image Credit: |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 William June 24, 2010 If you have a Razor product that is the subject of a recall, and your are not the original purchaser, don’t bother calling them for a replacement. Their recalls only apply to the original purchaser. I have a scooter that is under one of their recalls, but they will not help me with it simply due to the fact that I’m not the original purchaser. I was told to quit using it and destroy it. But they will not fix/replace the defective unit. Thanks, Bill 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 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)
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