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Johnson & Johnson’s Abiomed has issued another safety correction involving Automated Impella Controllers, the devices used to control and monitor Impella heart …

More Than 17,000 Recalled Coffee Makers Linked to Reports of Unexpected Steam and Hot Liquid Releases Causing First- and Second-Degree Burns What …

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 …