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.
Dorel Car Seat Recall Issued Due to Defective Safety Harness February 15, 2011 Staff Writers Add Your CommentsAbout 800,000 Dorel child safety seats are being recalled due to a problem with the harness and release button, which could pose a substantial risk of a child in the seat suffering an injury in the event of an auto accident.ย ย The Dorel car seat recall was announced on Monday by the National Highway Traffic Safety Administration (NHTSA), which began investigating reports of problems with the car seats last March.According to the NHTSA, the recalled child car seats have a release button on the harness that does not always return to the locked position. If the button is not locked, the harness adjustment strap can slip back through the adjuster if the child moves around, causing the harness to loosen.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 COMPENSATIONAlthough there have been no injuries reported in connection with the Dorel child safety seat problems, this could pose a substantial hazard for infants or young children.More than 50 models are included in the car seat recall by Dorel, including infant safety seats, booster seats, and convertible child safety seats sold alone or as part of a travel system with a stroller.All of the affected child safety seats were manufactured between May 1, 2008 and April 30, 2009, and have a โCenter Front Adjusterโ (CFA) on the harness. A complete list of models affected by the recall is available in the NHTSA recall report.The Dorel Juvenile Group (DJG) has announced plans to provide a repair kit to consumers who have the recalled child safety seats, which will include a non-toxic, food-grade lubricant that can prevent the CFA button from sticking, as well as instructions on how to properly apply it, and a label that indicates it has been repaired.The NHTSA says that parents who wish to continue to use the car seats can do so, but should make certain that the harness is properly adjusted and the lock/release button is in the fully locked position. Once the child is in the seat and adjustments are made, the caregiver should pull on the shoulder part of the harness to ensure it is secure and will not loosen, the NHTSA advised.Consumers with questions should contact DJG at 1-866-623-3139. Tags: Auto Accident, Car Seat Recall, Dorel Image Credit: |More Lawsuit Stories Apple AirTags Allowed Abusive Husband to Stalk, Control Wife, Lawsuit Alleges November 6, 2026 Snapchat Sexual Exploitation Lawsuit Alleges Disappearing Messages Helped Predators Groom Children November 6, 2026 Dupixent Cancer Lawsuit Alleges Eczema Treatment Accelerated Cutaneous T-Cell Lymphoma November 6, 2026 0 Comments X/TwitterThis 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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