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Parents and Caregivers Urged to Stop Using Recalled Dive Sticks That Violate Federal Safety Standards and Create Dangerous Impalement Hazards What Parker …

A Sharp Rise in Class I Medical Device Recalls Highlights Growing Risks for Patients Harmed by Defective Medical Devices What Parker Waichman …

What Parker Waichman LLP Found Recent 2026 baby product recalls involve bacterial contamination, choking hazards, suffocation risks, drowning hazards, fall hazards, fire …

Parents Nationwide Warned to Stop Using Certain Up & Up Baby Wipes Following Reports of Irritation, Infections, and the Presence of Burkholderia …

Johnson & Johnson MedTech Recall Raises Concerns About Blood Clot Formation, Vascular Complications, and Patient Safety During Critical Heart Procedures What Parker …

New Bipartisan Legislation Aims to Preserve Federal Limits on PFAS Chemicals as Regulatory Changes and Compliance Delays Generate Public Health Concerns What …

Consumers Across the United States Are Being Warned About Recalled Gas-X Products After the FDA Classified the Recall as a Class II …

More Than 120,000 Squishy Toys Sold at Walmart and Other Retailers Recalled After Reports That Sand Filling May Contain Fibrous Tremolite or …

More Than 10,000 Power Recliners, Sofas, and Loveseats Recalled After Reports of Overheating Switches, Smoke, Burning, and Fires. What Parker Waichman LLP …

FDA Class I Recall Involves Certain Relay Pro Thoracic Stent Grafts After Reports of Device Release Failure, Emergency Open Surgery, Stroke, Aortic …