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.
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
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.
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.
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.
Nuna Baby Essentials Recalls 600,000 Child Car Seats Over Loosening Harnesses: NHTSACar seat harnesses may not close completely, leaving children at risk of injury during a crash. December 20, 2024 Darian Hauf Add Your CommentsFederal highway safety officials have announced a recall of more than 600,000 Nuna Baby Essentials, Inc. child car seats due to a risk of the harness failing to properly restrain the child safely in the seat.The U.S. National Highway Traffic Safety Administration (NHTSA) announced the Nuna Baby child car seat recall on December 18, warning that certain Rava child car seats with a plastic harness adjuster button may lack a fabric covering, potentially allowing debris to enter the adjuster mechanism.Officials are warning that if debris enters the adjuster mechanism, it may prevent the teeth from gripping the adjuster strap securely. This can cause the harness to loosen, which may fail to properly restrain the child in the event of a crash, increasing the risk of injury.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 car seat recall impacts 608,786 Nuna Rava 9999 car seats with model numbers CS-50, CS05101, CS05103, CS05104, CS05105, CS05106, CS05107, CS05109, CS05110, CS05111, CS05114 and CS05115. The affected products were produced between July 16, 2016 and October 25, 2023.To avoid the potential for injuries, Nuna Baby Essentials advises caregivers to always check the harness tightness when placing their child in a car seat.While the company is unaware of any injuries or incidents related to the defect, there have been numerous complaints related to the harness loosening through the adjuster mechanism.NHTSA initiated an investigation in May 2024, after receiving a defect petition. On October 24, 2024, NHTSA opened an evaluation into the car seat defects.The manufacturer then decided to conduct a voluntary safety recall for all Rava child car seats manufactured in the designated time frame.Nuna plans to provide consumers with a free remedy kit, which includes a new seat pad, instructions for properly cleaning the harness adjuster area and installing the new seat pad, a screwdriver to remove and replace the plastic cover over the harness adjuster, and a plastic brush to clean the teeth of the harness adjuster and remove any debris.The new seat pad is designed to cover the plastic harness adjuster cover and help prevent debris from entering the mechanism.For more information, owners may contact Nuna customer service at 1-855-686-2891 or via email at info.usa@nunababy.com. Nunaโs contact for this recall is Emily C. Smith, who may be reached by email at emily.c.smith@dot.gov.Consumers may also contact the NHTSA vehicle safety hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.nhtsa.gov. Written by: Darian HaufConsumer Safety & Recall News WriterDarian Hauf is a consumer safety writer at AboutLawsuits.com, where she covers product recalls, public health alerts, and regulatory updates from agencies like the FDA and CPSC. She contributes research and reporting support on emerging safety concerns affecting households and consumers nationwide. Tags: Car Seat, Car Seat Recall, Child Car Seat, Harness Adjustor, Nuna Baby Essentials, Rava Car Seats Image Credit: Shutterstock: T. SchneiderMore Lawsuit Stories Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges August 11, 2026 Enfamil Necrotizing Enterocolitis Lawsuit Set for Trial to Begin This Week August 11, 2026 Gree Dehumidifier Lawsuit Alleges Defective Appliance Caused House Fire August 11, 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 Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026) Abbott Continues to Oppose Spinal Cord Stimulator Lawsuit MDL, Despite Mounting Claims (Posted: 2 days ago)Manufacturer wants the Judicial Panel on Multidistrict Litigation to reject a proposal by a group of plaintiffs to consolidate all federal Abbott spinal cord stimulator lawsuits.MORE ABOUT: SPINAL CORD STIMULATOR LAWSUITLawsuit Over Spinal Cord Stimulator Removal Claims Device Caused Numbness, Incontinence (08/06/2026)Spine Stimulator Injury Lawyers Seek Leadership Roles in Boston Scientific MDL (07/31/2026)Spinal Cord Stimulator Reprogramming Caused Electric Shocks, Worsening Pain: Lawsuit (07/27/2026) AngioDynamics SmartPort Infection Lawsuit Alleges Defective Port Caused Sepsis (Posted: 5 days ago)A Pennsylvania man has filed an AngioDynamics SmartPort lawsuit alleging catheter defects promoted bacterial growth, causing a severe infection and sepsis only weeks after implantation.MORE ABOUT: ANGIODYNAMICS PORT CATHETER LAWSUITPort Catheter Sepsis Lawsuit Claims Defective SmartPort Implant Caused Infection (07/22/2026)SmartPort Catheter Lawsuit Claims Defective AngioDynamics Port-a-Cath Caused Infection (07/14/2026)Vortex Port Lawsuit Claims Defective AngioDynamics Device Caused Infection, Pulmonary Embolism (07/07/2026)
Dupixent CTCL Studies Highlighted Cancer Risks For Years, Lawsuit Alleges (Posted: yesterday)A Dupixent CTCL lawsuit indicates manufacturers have long known the eczema treatment was linked to an increased cancer risk, but failed to warn doctors or patients.MORE ABOUT: DUPIXENT LAWSUITCTCL Lawsuit Alleges Diagnosis Came After Less Than a Year of Dupixent Use (07/29/2026)Lawsuit Alleges Dupixent Caused Mycosis Fungoides Diagnosis (07/21/2026)Dupixent MDL Judge To Meet With Lawyers for Initial Case Management Conference in October 2026 (06/25/2026)
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