The U.S. Food and Drug Administration (FDA) issued an alert on May 21, 2007.

The U.S. Food and Drug Administration (FDA) has issued advisories about this issue.

In December 2000, the U.S. Food and Drug Administration (FDA) issued a warning about these injuries.

In 2000, the U.S. Food and Drug Administration issued a black box label on nevirapine, warning that it could cause severe liver damage, including liver failure.

The U.S. Food and Drug Administration today issued final guidance for people who wish to comment during the agency's advisory committee meetings.

The U.S. Food and Drug Administration today issued a draft guidance aimed at fostering early-stage development of medical devices within the United States.

The U.S. Food and Drug Administration issued a consumer warning.

The U.S. Food and Drug Administration (FDA) issued a press release updating the available information.

The U.S. Food and Drug Administration (FDA) has issued an advisory to use this product exactly as labeled.

The U.S. Food and Drug Administration (FDA) has issued a consumer health warning about e-cigarettes.