NBC News medical contributor Dr. Natalie Azar reports on the FDA panel discussion of the use of antidepressants during ...

The FDA is sounding the alarm with a deodorant recall that is impacting more than 67,000 cases of antiperspirant made by a popular manufacturer.

The Republican-backed legislation targets specific dyes and preservatives linked to health concerns following California's ...

The FDA did not provide a reason for the recall, but said the products had a cGMP (Current Good Manufacturing Practices) ...

The Food and Drug Administration has recalled more than 67,000 cases of deodorant sold at major retailers due to manufacturing practices that violate federal regulations.

More than 100,000 ice cream bars were recalled by the Food and Drug Administration due to potential listeria contamination.

With so few Alzheimer's drugs available, repurposing medications approved for other conditions could be the key to tackling ...

The FDA said that it was recalled for cGMP deviations in the manufacturing process. The acronym means “Current Good Manufacturing Practice” and are the rules the FDA uses to make sure that a product ...

It's a good thing the U.S. Food and Drug Administration is staying on top of the latest recalls, because knowing about new recalls impacts people's lives. The sooner you find out about an item that ...

Children's Hospital Los Angeles, citing recent U.S. Food and Drug Administration actions, on Monday said it has paused usage of Sarepta Therapeutics' gene therapy Elevidys in all patients with ...

The Food and Drug Administration on Monday named George Tidmarsh, a longtime biotech executive who has a background in ...