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

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."

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.

Shaman Botanicals has issued a formal response to the FDA’s recent warning letter on its 7-hydroxymitragynine (7-OH) products, backed by reports from leading researchers at Johns Hopkins, Harvard, UCLA,

A nationwide recall of more than 40,000 units of toothpaste has received the lowest risk level by the Food and Drug Administration. A recall for Sensodyne Pronamel Active Shield Toothpaste for Sensitive Teeth began on August 5 over concerns that "Fresh Mint" tubes were mislabeled "Cool Mint/Whitening.

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,

With skin cancer cases up 77% since 1994, the bipartisan legislation seeks to address regulatory hurdles that have blocked new sunscreen ingredients for decades.

The U.S. Food and Drug Administration recently approved FluMist, a flu vaccine that can be ordered online and used at home.

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.