Storing food in a refrigerator or freezer that isn't cold enough can be dangerous. Prevent foodborne illness in your ...

The U.S. Food and Drug Administration has published the 2022 Food Code Supplement. The Supplement updates the 2022 Food ...

Recent modifications to FDA’s import alerts, as posted by the agency, are listed below. Use the chart below to view import alerts. The U.S. Food and Drug Administration responded to objections ...

The US Food and Drug Administration is moving ahead with a plan to overhaul its food safety efforts, despite a lack of new legal authorities and resources. As part of a reorganization that went ...

Now, the U.S. Food and Drug Administration (FDA) has given the recall its highest risk classification. A Class I recall, the highest risk level, is issued when there is a "reasonable probability ...

The agency said the risk level is based on food type, manufacturing process and the facility’s compliance history. “FDA inspectors are looking for temperature controls, cleanliness and ...

It’s been more than three years since DBV Technologies’ peanuty allergy therapy was rejected for FDA approval ... protein – one of the most common food allergies in children.

and drug-drug or drug-food interactions. Additionally, there are popular articles on common medication, latest pharma news, calculators, instructional videos, access to directory of pharmaceutical ...

It can all really leave you jonesing for a crisp apple cider. But, according to the Food and Drug Administration (FDA), you may want to be careful when you reach for that classic autumn drink.

Risk Disclosure: Trading in financial instruments and/or cryptocurrencies involves high risks including the risk of losing some, or all, of your investment amount, and may not be suitable for all ...

An ex-FDA employee has revealed what he claims is the most harmful breakfast cereal on the US market. Dr. Darin Detwiler, who previously served as a food safety expert for the agency, told the Dai ...

The recall has now been given a Class II risk definition by the U.S. Food and Drug Administration (FDA). A Class II recall is "a situation in which use of or exposure to a violative product may ...