The FDA recalled more than 64,000 pounds of Bunge North America's NH European Style Butter Blend due to potential undeclared ...

The U.S. Food and Drug Administration (FDA) has elevated the risk classification for a nationwide butter recall, now labeling ...

The same butter was recalled earlier in July, but only designated as a Class III.

The former official, Vinay Prasad, had been on the job three months and had recently come under attack by conservative ...

The FDA approved aceclidine 1.44% ophthalmic solution (Vizz) for adults with presbyopia, or age-related blurred near vision, ...

The FDA will soon require prescription opioid manufacturers to include stronger language on the medications’ labels warning ...

The FDA is mandating new labeling for opioids to better inform patients and healthcare providers about the risks of addiction ...

Bunge North America Inc. initiated a voluntary recall of 64,800 pounds of butter due to a potential undeclared allergen.

Dr. Vinay Prasad, an oncologist who was a fierce critic of COVID vaccine and mask mandates, was appointed in May.

The new rule comes after a public advisory committee meeting in May that reviewed data showing risks for patients who use opioids over long periods. Those risks include misuse, addiction and overdoses ...

OH, a kratom derivative, is marketed as a natural remedy, but the FDA says it’s dangerous. About the hidden risks and what ...