A Class I recall is used when "a violative product will cause serious adverse health consequences or death," according to the FDA.

The Malaysian health ministry says Facebook posts promoting a gel to treat bone and joint pains are "fake" and the accounts ...

With over 27 years of export experience, Vinamilk is one of the few companies with significant advantages as the Halal market ...

A sign with the company logo stands in front of the Eli Lilly and Company headquarters campus in Indianapolis, Indiana, on March 17, 2024. New study data has solidified the club's position Eli Lillyis ...

The FDA is weighing a ban on red dye No. 3, a synthetic dye used in some foods and drinks after concerns have been raised ...

The risk of cross contamination has long been recognized by cosmetic companies. But recent FDA-sponsored testing hasn't uncovered any safety issues. Since 2021, laboratory analysis of more than ...

Whole grains and fruits are in, and added sugar is out. That’s going to change what’s on a lot of cereal boxes and other things ...

As of Dec. 26, there were 31 patients in the outbreak. The FDA has not reported where the patients live. The agency has begun traceback efforts, but has not yet reported what food it is tracing.

The agency updates and modifies the alerts as needed. 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 (FDA) recently finalized its long-awaited rule redefining the use of the term “healthy” on food packaging.

(RTTNews) - BeiGene (BGNE) announced the FDA has approved TEVIMBRA, in combination with platinum and fluoropyrimidine-based chemotherapy, for the first-line treatment of unresectable or metastatic ...