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.
Honda FourTrax ATV Recall Issued Over Defective Suspension Arms February 22, 2012 Staff Writers Add Your CommentsAbout 2,900 Honda FourTrax All-Terrain Vehicles (ATVs) have been recalled following reports of suspension arm failures, which could cause the vehicle to crash.ย The Honda FourTrax ATV recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on February 21, after the manufacturer received at least four reports of suspension arm weld failures. At least one rider has been injured, suffering a sprained wrist in an ATV accident.According to the CPSC, the upper front right suspension arm weld can fail, which can cause the driver to lose control of the ATV.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 ATV recall affects about 2,900 two-wheel drive 2012 Honda FourTrax Ranger ATVs with model numbers TRX420TE and TRX420TM. The affected TRX420TE models have Vehicle Identification Numbers (VINs) of 1HFTE344* C4500841 through C4502580 and the affected TRX420TM models have VINs of 1HFTE340* C4500542 through C4501681, the * representing 0-9 or an X. The model number is located on the right frame down pipe over the front right side wheel. The VIN is on the top center front of the frame between the bars of the gear rack and through the middle opening of the front fairing.The recalled ATVs were sold at Honda ATV dealers nationwide for between $5,100 and $5,300 from September 2011 through January 2012.The CPSC recommends that consumers stop using the recalled ATVs immediately and contact their Honda ATV dealer to schedule a free repair. Consumers with questions can call American Honda at (866) 784-1870 or visit the company’s website at http://powersports.honda.com. Tags: ATV, ATV Accident, ATV Recall, HondaMore Lawsuit Stories SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body May 15, 2026 Therapeutic Heating Pad Lawsuit Alleges Amazon Device Overheated, Burned User May 15, 2026 FDA Issues Additional Tazverik Blood Cancer Warnings After Market Recall May 15, 2026 1 Comments Jimmy October 10, 2012 I have a 2012 honda rancher 4/4 and the weld on the a arm broke on my atv I think that honda should of checked all there atvs when they first found out of there problems with the welds on there 2012 models. They don’t want to spend any money to fix there screw up somebody is serious gonna get hurt my atv was bought less than two months ago PhoneThis 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 SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 3 days ago)A Missouri woman alleges her AngioDynamics SmartPort catheter fractured and left a broken piece near her heart, requiring surgical removal after it was found during a CT scan.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUIT18 AngioDynamics Port Catheter Lawsuits Will Be Selected for Bellwether Discovery in August 2026 (05/05/2026)AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism (04/30/2026)Vortex Port Lawsuit Filed After Port Catheter Removed Due to Infection, Blood Clots (04/09/2026) Enfamil NEC Lawsuit Cleared For MDL Trial in July 2026 (Posted: 4 days ago)A federal judge has selected an Enfamil lawsuit to serve as the first NEC infant formula bellwether trial, which is set to begin in July.MORE ABOUT: ENFAMIL AND SIMILAC BABY FORMULA LAWSUITLawsuit Claims Cowโs Milk-Based Baby Formula Use Resulted in Infant Suffering Devastating NEC Symptoms (05/08/2026)Mead Johnson Lawsuit Claims Premature Child Developed NEC From Enfamil (04/24/2026)Similac NEC Lawsuit Payout Increased by $17M in Punitive Damages (04/14/2026) Abbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (Posted: 5 days ago)According to a lawsuit brought against the manufacturer and the FDA, an Abbott Eterna spinal cord stimulator has caused pain, shocks and complications instead of the relief promised.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITNevro 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)JPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)
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