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.
Ski-Doo Snowmobile Recall Issued Amid Reports of Fires, Fuel Leaks February 8, 2013 Russell Maas Add Your CommentsAbout 10,200 Ski-Doo snowmobiles have been recalled due to problems with the fuel pump fitting, which may come in contact with the oil tank and cause a fuel leak or fire.ย The Ski-Doo Snowmobiles recall was announced by the U.S. Consumer Product Safety Commission on February 7, after the manufacturer received at least three reports of fires starting because the fuel pump inlet fitting made contact with the oil tank, causing it to break and leak fuel. To date, no injuries have been reported in connection with fires with the snowmobiles.The recall includes various 2013 Ski-Doo snowmobile models with model names Freeride, Grand Touring, DSX, MXZ, Renegade, Skandic, and Summit. For a full list of recalled models and model numbers consumers may visit http://www.cpsc.gov/en/Recalls/2013/BRP-Recalls-Ski-Doo-Snowmobiles/.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 recalled Ski-Doo snowmobiles were manufactured in Canada by Bombardier Recreational Products Inc., of Valcourt, Canada and sold at Ski-Doo dealers nationwide from March 2012 through January 2013 for between $8,000 and $12,000.Similar problems led to an Arctic Cat snowmobile recall in December, which affected 3,900 vehicles. That recall was issued following reports of leaking fuel tanks, with the manufacturer, Arctic Cat Inc., indicating that the faulty fuel tanks sustained damage during the manufacturing process.In Januaryย 2012, Arctic Cat Inc. recalled another 19,000 snowmobiles due to steering tie rods becoming dislodged causing at least four reports of steering loss including one report resulting in complete loss of control, posing a crash hazard to the driver.Consumers with recalled Ski-Doo snowmobiles should immediately stop using the products and contact a BRP dealer at (888) 638-5397 to schedule a free repair. Consumers with questions can also visit the company’s website at www.ski-doo.com. BRP has begun notifying registered consumers directly about the recall and necessary repair. 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: Ski-Doo, Snowmobile, Snowmobile Recall Image Credit: |More Lawsuit Stories Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss May 21, 2026 Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026 Lawsuit Alleges Boston Scientific Urinary Sphincter Failed, Required Additional Surgery May 21, 2026 0 Comments 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 Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss (Posted: today)A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.MORE ABOUT: OZEMPIC LAWSUITOzempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk (05/14/2026)Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (05/04/2026)GLP-1 Dementia, Alzheimerโs Disease Risks Questioned in New Study (04/27/2026) Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (Posted: yesterday)According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITLawsuit 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)Judge Says Suboxone โSchedule Aโ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026) Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: 2 days ago)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)
Bard Ventralex Patch Lawsuit Claims Umbilical Hernia Mesh Failed, Requiring Removal Surgery May 21, 2026
Mounjaro NAION Lawsuit Claims Side Effects Led to Permanent Vision Loss (Posted: today)A Mounjaro vision loss lawsuit accuses Eli Lilly of failing to properly investigate the drug’s side effects and provide proper warnings before marketing it to the public.MORE ABOUT: OZEMPIC LAWSUITOzempic and Mounjaro Drug Class Linked to 35% Higher NAION Vision Loss Risk (05/14/2026)Ozempic Vision Loss Lawsuit Highlights Devastating Consequences of NAION Diagnosis (05/04/2026)GLP-1 Dementia, Alzheimerโs Disease Risks Questioned in New Study (04/27/2026)
Suboxone Oral Film Lawsuit Claims Opioid Treatment Causes Tooth Decay (Posted: yesterday)According to a recently filed lawsuit, exposure to Suboxone oral film strips caused an Illinois man to suffer severe tooth decay that required extensive dental work.MORE ABOUT: SUBOXONE TOOTH DECAY LAWSUITLawsuit 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)Judge Says Suboxone โSchedule Aโ Lawsuits Should Be Filed Individually or Dismissed (04/27/2026)
Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: 2 days ago)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro Stimulator Lawsuit Alleges SCS Lead Failure Caused Nerve Damage (05/06/2026)Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (04/29/2026)