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.
Graco Car Seat Recall Impacts 3.7 Million Harness Buckles February 12, 2014 Russell Maas Add Your CommentsRoughly 3.7 million Graco car seats are being recalled due to a risk that the harness buckles may jam and trap children in a car during an emergency. ย The Graco recall was announced by the National Highway Traffic Safety Administration (NHTSA) on February 11, following an investigation prompted by multiple complaints that suggested the buckles may become difficult to unlatch over time.Although no injuries have been reported to date, the defective Graco car seat buckles may pose a serious risk in the event of an emergency. The manufacturer acknowledges that food and liquids may become lodged in the buckle’s groove, making it difficult to unlatch by pressing the red release button. If this occurs, it can make removing the child from the seat problematic or even impossible in the event of an emergency.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 Graco car seat models included in the recall are Toddler Convertible car seats, Cozy Cline, Comfort Sport, Classic Ride 50, My Ride 65, My Ride 70, My Ride 65 with Safety Surround, Size4Me 70, My Size 70, Head Wise 70, Smart Seat, Nautilus 3-in-1, and Nautilus Elite and Argos models.The affected models were manufactured under the Graco brand name and sold nationwide from 2009 through July 2013, with a suggested retail prices between $99.00 and $399.00.According to the NHTSA, Graco declined to recall seven other models of car seats that may pose the same hazard, rejecting a formal request by the federal safety agency that they be added to the recall. Those models include Snugride, Snugride 30, Snugride32, Infant Safe Seat-Step 1, Snugride 35, Tuetonia 35, and Snugride Click Connect 40. Although Graco is not recalling those car seats, the NHTSA is advising customers with these models to still report any adverse events that may occur.Graco announced in the recall that regular cleaning of the belt buckles will help prevent the chances of the buckles becoming stuck. Placing the buckle in a cup of warm water and pressing the red release button may help to dislodge any dried particles.Graco also announced the potential problems for the buckle to unlatch does not in any way prevent the effectiveness of the car seat or the restraining of the child. However, the NHTSA has advised for parents to find an alternative car seat with restraints until a replacement or repair kit is provided.Customers with affected car seats should contact Graco at 800-345-4109 or by email at consumerservices@gracobaby.com to receive a โnew and improved replacement harnessโ at no cost. 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: Auto Accident, Car Seat, Car Seat Recall, Graco Image Credit: |More Lawsuit Stories NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction May 1, 2026 Lawsuit Indicates Dupixent Lymphoma Diagnosis Resulted in Multiple Rounds of Chemotherapy May 1, 2026 Medtronic Azure Lawsuit Claims Pacemaker Caused Heart Arrhythmias May 1, 2026 0 Comments EmailThis 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 NFL Sports Gambling Lawsuit Claims Live Game Data Fueled FanDuel, DraftKings Addiction (Posted: 2 days ago)A public health advocacy group and two Pennsylvania men have filed a lawsuit against FanDuel, DraftKings and the NFL over the use of data for addictive, live in-game microbets.MORE ABOUT: SPORTS BETTING ADDICTION LAWSUITAppeal Challenges Dismissal of DraftKings Lawsuit Over Gambling Addiction (04/27/2026)BetMGM Lawsuit Alleges Gambling Addictโs โSelf-Exclusionโ Listing Was Not Honored (04/13/2026)DraftKings Settlement Reached in Lawsuit Over MLB Gambling Promotions (04/10/2026) Recalled Omnipod 5 Injuries Skyrocket, Prompting Removal of Insulin Pump Pods (Posted: 3 days ago)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: 4 days ago)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)
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