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.
Dynacraft Motor Scooter Recall Issued Due to Fall Hazard February 27, 2013 Russell Maas Add Your CommentsAbout 10,700 battery operated motor scooters sold at Walmart and Toys ‘R’ Us are being recalled due to problems where the scooters may accelerate suddenly during use, posing a serious injury risk for young riders and bystanders.ย A Dynacraft Monster scooter recall and Hello Kitty High City motor scooters recall were announced by the U.S. Consumer Product Safety Commission (CPSC) on February 26, after the manufacturer received at least nine reports of the scooters accelerating at random during use. At least three injuries have been linked to the sudden acceleration.The Dynacraft motor scooter recall consists of 5,500 purple and black colored scooters with Monster High graphics located on the front panels and rear fenders. The Monster High models were manufactured between October 5, 2012 and November 7, 2012 with the model number 8801-14 and serial code QYCEI followed by a six digit number ranging between 0031215 and 014456. The manufacture date, serial, and model numbers can be located on the underside of the scooters on the center platform.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 COMPENSATIONA separate recall for Dynecraft Hello Kitty scooters involves 5,200 pink and black colored motor scooters with Hello Kitty graphics on the front panels, footboard and rear fenders. The Hello Kitty models were manufactured between September 10, 2012 and December 3, 2012 with model number 8801-03 and serial code QYCEI followed by a six digit number ranging between 000001 and 014456. The manufacture date, serial and model numbers can be located underneath of the scooter on the center platform.Both recalled models were manufactured in China by Zhejiang Qunying Vehicle Co. LTD and distributed by Dynacraft BSC Inc., of American Canyon, California. The Hello Kitty models were sold exclusively at Toys R Us stores and on toysrus.com nationwide from October 2012 to January 2013 for about $279. The Monster models were sold exclusively at Walmart stores and Walmart.com nationwide from November 2012 to January 2013 for about $249.The CPSC recommends consumers stop using the recalled electric, battery powered scooters immediately, disconnect the battery and return it to the nearest Walmart or Toys R Us (depending upon model) to receive a full refund or store credit. Consumers may also call Dynacraft at (800) 551-0032 from 7a.m. to 4p.m. PT Monday through Friday or visit the company’s website online at www.dynacraftbike.com and navigate to Owners then Warning/Recalls. 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: Accident, Childrens Toy, Toys R Us, Walmart Image Credit: |More Lawsuit Stories Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026 Dupixent Side Effects Caused CTCL, Tumors, Lawsuit Alleges September 10, 2026 LG Electric Range Lawsuit Alleges Defective Controls Caused House Fire September 10, 2026 0 Comments InstagramThis 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 Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026) Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026) Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit September 10, 2026
Abbott Spinal Cord Stimulator Explant Surgery Required After Device Failure: Lawsuit (Posted: today)A South Carolina woman alleges an Abbott spinal cord stimulator malfunction caused painful electrical shocks that required removal surgery less than two years after implantation.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITBoston Scientific Spinal Cord Stimulator Lead Recall Issued After More Than 1,000 Serious Injuries (09/04/2026)Judge Allows Back Stimulator Lawsuits Against Boston Scientific to Be Directly Filed in MDL (08/31/2026)Hearing on Abbott, Nevro SCS Lawsuit MDL Centralization Set for September 2026 (08/26/2026)
Jury Awards $40M Port Catheter Lawsuit Payout in Bard PowerPort Bellwether Trial (Posted: yesterday)The second Bard PowerPort lawsuit bellwether trial has ended in a $40 million verdict for the plaintiff who had the implant removed after the catheter broke and traveled to her heart.MORE ABOUT: BARD POWERPORT LAWSUITNearly 4,000 Bard PowerPort Lawsuits Are Awaiting Outcome of Upcoming Bellwether Trials (08/12/2026)Bard PowerPort Lawyers Make Final Preparations for Next MDL Bellwether Trial (07/17/2026)New Trial Sought for First Bard PowerPort Bellwether Lawsuit (06/05/2026)
Lawsuit Alleges Ozempic Caused Sudden Eyesight Loss (Posted: 2 days ago)An Ozempic NAION lawsuit blames the diabetes drug for a woman’s sudden loss of vision and alleges the manufacturer failed to warn doctors of the risks.MORE ABOUT: OZEMPIC LAWSUITOzempic NAION Lawsuit Filed Over Sudden, Permanent Vision Loss (08/03/2026)Link Between NAION and Ozempic, Wegovy Will Be Focus of Early Discovery in GLP-1 Vision Loss Lawsuits (07/16/2026)Wegovy Vision Side Effects Resulted in Blindness in Left Eye, Lawsuit Alleges (06/16/2026)