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.
TOMY Boon Highchair Recall Issued After Dozens of Falls, Infant InjuriesThe manufacturer has received numerous reports of the highchairs separating from their bases, resulting in the chairs, and the children in them, falling over. September 5, 2023 Martha Garcia Add Your CommentsMore than 85,000 TOMY highchairs have been recalled, following reports of problems where the seat suddenly separated from the pedestal base, resulting in at least two dozen incidents where children fell from the highchairs, often suffering injuries, bruises and scratches.The U.S. Consumer Product Safety Commission (CPSC) announced the TOMY highchair recall on August 31, indicating that the bolts used to secure the seat to the pedestal base can become loose and allow the seat to detach. This can pose a fall hazard to the child occupant inside.TOMY has received 34 reports of the chair separating from the base, which has resulted in reports of at least 24 falls and 11 child injuries.The recall includes Boon Flair highchairs manufactured before September 2016 and all Boon Flair Elite highchairs manufactured at any time. The Flair Elite has a white and orange molded plastic seat with a white tray and metal pedestal base. Flair highchairs have a gray plastic pedestal base and were sold in 10 color combinations, including blue/white, white/orange, pink/white, green/white, gray/green, white, gray, white/gray, white/blue, and red/white. The recall includes model numbers B751, B701โB709, B716โB718, B731, B10147, B11068, B11069, and B11401.Consumers can check the model number and manufacturing date code printed on the label located under the base of the highchair.According to the recall notice, about 83,000 of the recalled highchairs were sold in the U.S., with another 2,850 sold in Canada. They were manufactured in China and distributed by TOMY, based in Oak Brook, Illinois.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 highchairs were sold at Bed Bath & Beyond, Target, Toys โRโ Us, and other stores nationwide, as well as online at Amazon.com, Target.com, Walmart.com, and BedBathAndBeyond.com.Flair Elite highchairs were sold from 2008 to 2009 for about $380. The Flair models were sold from January 2008 through February 2017 for between $230 and $250.The CPSC recommends consumers stop using the affected highchairs immediately and contact TOMY for a free repair kit. The repair kit will include a set of bolts and split and flat washers to repair the recalled highchair.Consumers with questions about the recall should contact TOMY at 866-725-4407 or online at https://recall.tomy.com. Written by: Martha GarciaHealth & Medical Research WriterMartha Garcia is a health and medical research writer at AboutLawsuits.com with over 15 years of experience covering peer-reviewed studies and emerging public health risks. She previously led content strategy at The Blogsmith and contributes original reporting on drug safety, medical research, and health trends impacting consumers. Tags: Child Injury, Fall, High Chair RecallMore Lawsuit Stories Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods April 30, 2026 Weber Grill Brush Lawsuit Claims Detached Bristle Punctured Manโs Intestine April 30, 2026 AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 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 Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026) Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: yesterday)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026) Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 2 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)
AngioDynamics Catheter Lawsuit Claims SmartPort Device Embedded in Jugular Vein, Caused Embolism April 30, 2026
Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: today)Insulet is removing certain Omnipod 5 insulin pump pods from use following a surge in reports of insulin delivery failures that raise risks of diabetic ketoacidosis and other serious complications.MORE ABOUT: OMNIPOD RECALL LAWSUITInsulet OmniPod 5 Recall Lawsuits May Be Filed Over Problems Resulting in Diabetic Ketoacidosis, Hospitalization and Death (03/24/2026)Omnipod 5 Insulin Pump Recall Follows Reports of Serious Injuries: FDA (03/20/2026)
Lawsuit Claims Abbott, Boston Scientific SCS Pre-Market Approval Supplements Caused Permanent Injuries (Posted: yesterday)A Florida womanโs lawsuit alleges that Abbott Laboratories and Boston Scientific altered their SCS device batteries, firmware and stimulation features without adequate safety testing approved by the FDA.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITJPML Sets Hearing Over Spinal Cord Stimulator Lawsuit Consolidation for May 28 (04/24/2026)SCS Injury Lawsuit Alleges Unlicensed Abbott Representatives Modified Device After Implantation (04/20/2026)WaveWriter Alpha Lawsuit Claims Defective Spinal Cord Stimulator Caused Pain and Surgical Removal (04/14/2026)
Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (Posted: 2 days ago)A Depo-Provera lawsuit filed against Pfizer says the manufacturer knew Depo-Provera could stimulate brain tumor growth before the birth control shots hit the market, yet failed to warn doctors and patients.MORE ABOUT: DEPO-PROVERA LAWSUITDepo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)Hearings on Evidence That Depo-Provera Causes Meningioma Brain Tumors Set for Late June 2026 (04/15/2026)High-Risk Brain Tumor From Depo-Provera Requires Frequent Monitoring, Lawsuit Claims (04/06/2026)