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.
Fisher-Price High Chair Recall Issued After Child Suffers Skull Fracture March 25, 2009 AboutLawsuits Add Your CommentsAbout 24,000 Fisher-Price 3-in-1 high chairs have been recalled due to a defective design of the booster seat release, which could cause the seat back to detach or fall backwards, posing a potential fall hazard.At least one report of problems with the Fisher-Price high chair seat back has been received, involving a young child who suffered a skull fracture in a fall.The defective Fisher-Price high chairs were sold exclusively at Target stores between December 2008 and March 2009 for about $100.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 product was marketed as a Fisher-Price “3-in-1 High Chair to Booster,” which contains a removable tray, adjustable seat and converts from a high chair to a booster seat.The high chair recall applies to units that have the product number P5369 printed on the side of the seat, on a label on the seat pad and on the high chair’s packaging.There are two main defects in the product. The first involves the booster seat release becoming unlatched while the child is in the chair, causing the seat to fall backwards. The second involves the seatback detaching if it is not fully snapped into place. Both of these problems may cause the child to fall out of the high chair and cause injuries that could be serious.ย Parents have been urged to stop using the Fisher-Price high chairs and to contact the manufacturer at (800) 432-5437 to request a free repair kit and instructions. Additional information can also be obtained at www.service.mattel.com. Tags: Baby Chair, Childrens Furniture, Fisher-Price, High Chair Recall, Target Image Credit: |More Lawsuit Stories Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit May 19, 2026 Cartiva Toe Implant Erosion Resulted in Persistent Pain, Lawsuit Alleges May 19, 2026 Amazon Ladder Collapse Lawsuit Claims Defective Device Caused Permanent Injuries May 19, 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 Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: today)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro 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) Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026) SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 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)
Abbott Spinal Cord Stimulator Problems Resulted in Severe Paralysis: Lawsuit (Posted: today)A man who became paralyzed has filed an Abbott spinal cord stimulator lawsuit after the original device failed, causing him to suffer electric shocks.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITAbbott Eterna Lawsuit Alleges Spinal Cord Stimulator Malfunction Resulted in Worsening Pain (05/13/2026)Nevro 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)
Depo-Provera Lawsuit Filings Exceed 6,000, As Court Prepares for First Test Trials (Posted: yesterday)The number of Depo-Provera lawsuits continues to climb, with more than 6,000 claims now filed nationwide by women who allege they developed brain tumors after receiving the birth control injections.MORE ABOUT: DEPO-PROVERA LAWSUITIntracranial Meningioma from Depo-Provera Shots Caused Hearing Loss, Vision Loss: Lawsuit (05/12/2026)Lawsuit Blames Depo Shot for Brain Tumors, Intense Headaches (04/28/2026)Depo-Provera Meningioma Warning Update Should Be Added to Birth Control Shot: Lawsuit (04/22/2026)
SmartPort Surgery Lawsuit Claims AngioDynamics Catheter Fractured Inside Womanโs Body (Posted: 4 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)