System integrates glucose biosensor with an AI-driven platform to show how food, activity, stress, sleep affect the body in real time

The Food and Drug Administration has authorized emergency use of animal drugs to treat and prevent infestations of the New World Screwworm, which poses an emerging threat to U.S. livestock and food security.

The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it has in the past.

The FDA cleared the first glucose monitoring system specifically designed for weight management from Signos, providing a new option for maintaining a healthy weight. The system uses a continuous glucose monitor,

FDA recalls 7Up Zero Sugar Tropical Soda for being mislabeled full-sugar soda. The affected cans were sold in 12-packs in Alabama, Florida and Georgia. This was just classified as a Class II recall, meaning it may cause reversible health effects.

By Sneha S K and Bageshri Banerjee (Reuters) -The U.S. Food and Drug Administration on Thursday approved Ionis Pharmaceuticals' drug to prevent instances of severe swelling in various parts of the body of patients with a rare genetic disorder.

The FDA classifies this recall as Class II, which the agency describes as a situation "in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."