Call to Action. In a letter dated July 9, 2025, the U.S. Food and Drug Administration (FDA) issued a clear call to action for ...

The US Food and Drug Administration warned that trendy whipped sunscreens made by Supergoop! and other manufacturers don’t ...

A sugar-free sweetener received the second-highest warning from the U.S. Food and Drug Administration. NuNaturals Inc. was ...

Shang Hao Jia Inc. issued a voluntary recall for select lots of three varieties of soda biscuits following a labeling error.

Distinctive Foods LLC issued a voluntary recall on July 25 for a select lot of crackers due to possible undeclared sesame.

The US Food and Drug Administration recently announced the launch of a regulatory incentive program pilot program, the ...

A first-in-class reversible dipeptidyl peptidase-1 (DPP-1) inhibitor, brensocatib addresses the underlying inflammatory ...

Approved in 2022, Skysona is indicated to slow the progression of neurologic dysfunction in boys 4 to 17 years of age with early, active cerebral adrenoleukodystrophy.

The FDA is requiring opioid pain medication manufacturers to update safety labeling with a stronger emphasis on risks from ...

A pair of sweeteners are being recalled nationwide due to a labeling mishap, according to the Food and Drug Administration ...

The Food and Drug Administration July 31 announced that it is requiring safety label changes to all opioid pain medications ...

The U.S. Food and Drug Administration plans to require new labels on all opioid pain medications that emphasizes long-term ...