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.
Family Dollar Store Toy Dart Gun Recall Issued After Two Choking Deaths May 19, 2010 Staff Writers Add Your CommentsAbout 1.8 million Family Dollar “Auto Fire” toy dart gun sets are being recalled after two young boys reportedly choked to death on the darts. The retailer is taking this action because the manufacturer has refused to recall the toy dart guns, despite the deaths and safety risk posed to other children. The toy dart gun recall was announced on Monday by the U.S. Consumer Product Safety Commission (CPSC), which has determined that the toys represent an asphyxiation hazard for children. The two victims included a 9-year-old boy from Chicago, Illinois, and a 10-year-old boy from Milwaukee, Wisconsin.The toy dart gun sets were made by Henry Gordy International, Inc., of Plainfield, New Jersey and were sold exclusively through Family Dollar. However, Henry Gordy refused to issue the recall after the boys’ deaths were reported, and Family Dollar stepped in to assist the CPSC with the recall instead, the CPSC announcement states.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 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 COMPENSATIONThe dart gun recall affects the “Auto Fire” toy gun and target sets, which included either an orange and yellow toy gun, or a blue and yellow toy gun, eight orange darts and a small dart board-styled target. The orange and yellow toy guns have an item number of #P238 and the blue and yellow guns have an item number of #9328. The item numbers can be found on the handle in raised lettering. The packages have “Gordy Toy” and “Ages 8+” on the packaging.The toy dart gun sets were sold at Family Dollar stores nationwide for $1.50 from September 2005 through January 2009.The announcement is the second major recall of toy dart gun sets in recent months. In December, the CPSC announced the recall of “Action Team” toy sets by OKK International, which were sold at discount stores nationwide. That recall was announced after an 8-year-old boy from Port Arthur, Texas, choked to death.The CPSC recommends that anyone who has one of these dart sets should immediately take them from children and either discard them or return them to Family Dollar for a full refund. Anyone with questions can visit the company’s website at www.familydollar.com. Tags: Childrens Toy Recall, Dart GunMore Lawsuit Stories Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations June 24, 2026 Polymarket Gambling Lawsuits To Be Consolidated Into Single Class Action June 24, 2026 Meta Lobbies Lawmakers for Social Media Addiction Lawsuit Immunity June 24, 2026 0 Comments 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 Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: today)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026) AngioDynamics Port Catheter Lawsuit Claims Woman’s SmartPort Implants Caused Multiple Infections (Posted: yesterday)A Georgia woman has filed an AngioDynamics port catheter lawsuit alleging two SmartPort implants caused repeated infections requiring multiple surgeries.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITXcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Woman’s Body (05/15/2026) Paraquat MDL Judge Requires Settlement Holdouts To Meet With Special Master (Posted: 2 days ago)Plaintiffs who have yet to decide to participate in a Paraquat lawsuit settlement agreement must meet with a Special Master overseeing negotiations within the next 30 days.MORE ABOUT: PARAQUAT PARKINSON’S DISEASE LAWSUITSInformation on Paraquat Settlement Offers To Be Provided to Special Master, MDL Judge Orders (04/09/2026)As Paraquat Parkinson’s Disease Cases Continue To Emerge, Syngenta Will Halt Herbicide’s Production (03/09/2026)Risk of Parkinson’s Disease From Paraquat Lead to Calls To Ban Weed Killer (02/11/2026)
Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations June 24, 2026
Lawsuit Alleges WaveWriter Alpha Spinal Cord Stimulator Problems Caused Burning, Shocking Sensations (Posted: today)Boston Scientific faces a lawsuit from a man whose WaveWriter Alpha spinal cord stimulator allegedly failed, causing burning sensations and electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Spinal Cord Stimulator Battery Problems Led to Repeat Surgeries, Lawsuit Claims (06/16/2026)Lawsuit Alleges Spinal Cord Stimulator Shocks, Burns Caused by Manufacturing Defect (06/12/2026)Boston Scientific Stimulator Lawsuits Centralized in Federal MDL (06/08/2026)
AngioDynamics Port Catheter Lawsuit Claims Woman’s SmartPort Implants Caused Multiple Infections (Posted: yesterday)A Georgia woman has filed an AngioDynamics port catheter lawsuit alleging two SmartPort implants caused repeated infections requiring multiple surgeries.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITXcela Port Lawsuit Claims AngioDynamics Catheter Caused Thrombosis (06/12/2026)Port Catheter Thrombosis Lawsuit Claims Defective AngioDynamics Xcela Device Caused Injury (06/03/2026)SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Woman’s Body (05/15/2026)
Paraquat MDL Judge Requires Settlement Holdouts To Meet With Special Master (Posted: 2 days ago)Plaintiffs who have yet to decide to participate in a Paraquat lawsuit settlement agreement must meet with a Special Master overseeing negotiations within the next 30 days.MORE ABOUT: PARAQUAT PARKINSON’S DISEASE LAWSUITSInformation on Paraquat Settlement Offers To Be Provided to Special Master, MDL Judge Orders (04/09/2026)As Paraquat Parkinson’s Disease Cases Continue To Emerge, Syngenta Will Halt Herbicide’s Production (03/09/2026)Risk of Parkinson’s Disease From Paraquat Lead to Calls To Ban Weed Killer (02/11/2026)