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.
Chlorpyrifos Parkinsonโs Disease Lawsuit Chlorpyrifos lawsuits are being investigated for individuals diagnosed with Parkinsonโs disease after direct, residential, occupational or Gulf War pesticide exposure.
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.
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.
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.
Gas-Powered Lawn Mower Recall Impacts 235K Mowers That May Fail to Turn Off October 19, 2016 Russell Maas Add Your CommentsNearly a quarter million gas-powered lawn mowers have been recalled, after the manufacturer received dozens of reports that suggest the engines may not shut off when the control bar is released, which poses a serious risk for users and bystanders.ย A Husqvarna walk-behind gas powered lawn mower recall was announced by the U.S. Consumer Product Safety Commission (CPSC) on October 18, impacting mowers sold under the brand names Craftsman, Poulan Pro, Jonsered, Craftsman, Yardworks, Murray, Brute and Husqvarna.The action was taken after at least 53 consumer reports indicating the engine and deck blades did not turn off after releasing the operator presence control bar safety feature. To date, no injuries have been reported.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 lawn mowers are equipped with an operator presence control bar that must be pressed down against the handlebar to engage the engine and mower deck blades. This safety feature is designed to disengage the mower and blades if the operator loses control of the handle to prevent laceration injuries.The recall includes certain lawn mowers equipped with Briggs& Stratton 7.25 horsepower engines, which are marked with serial numbers ranging between 110115M00001 and 082516M50000. Serial numbers and model numbers can be located on the rear of the mower deck next to the wheel. For a full list of the recalled model numbers please visit the CPSC recall notice.The push mowers are designed with either four similar wheels or two larger rear wheels and two smaller front wheels, an extended handle with an operator presence control bar, mowing deck, and with or without a collection bag. They were sold in various colors, including red, orange, yellow and black, or blue and have the Briggs & Stratton logo printed on the engine shield.According to the CPSC, an estimated 208,000 recalled lawn mowers were sold throughout the United States and an additional 27,000 were distributed for sale in Canada.The recalled lawn mowers were manufactured in the United States under Husqvarna Consumer Outdoor Products N.A. Inc. of Charlotte, North Carolina. They were sold at Loweโs, Sears and various other hardware stores, home centers and equipment dealers nationwide from November 2015 through August 2016 for between $250 and $450.Customers are being asked to stop using the recalled mowers immediately and contact Husqvarna at 877-257-6921 or email them at recalls@husqvarna.com for information on how to determine if the mower is in need of a free repair. Customers may also visit the manufacturers recall for further information at http://husqvarna.custhelp.com/app/answers/detail/a_id/1255/. 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: Craftsman, Husqvarna, Laceration, Lawn Mower, Lawn Mower RecallMore Lawsuit Stories Apple AirTag Stalking Lawsuits Consolidated in Northern District of California October 8, 2026 Kratom Overdose Lawsuit Alleges Krave Products Caused Fatal Mitragynine Intoxication October 8, 2026 Trifecta GT Heart Valve Lawsuit Alleges Premature Failure Led to Patientโs Death October 8, 2026 0 Comments CompanyThis 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. 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