U.S. Food and Drug Administration
The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by …
What We Do | FDA
FDA fulfills this responsibility by ensuring the security of the food supply and by fostering development of medical products to respond to deliberate and naturally emerging public health …
Drug Safety and Availability | FDA
Advances in FDA's Drug Safety Programs (annual reports) Index to Drug-Specific Information FDA Drug Safety Podcasts FDA’s Labeling Resources for Human Prescription Drugs …
Novel Drug Approvals for 2025 | FDA
Nov 3, 2025 · To see the FDA-approved conditions of use [e.g., indication (s), population (s), dosing regimen (s)] for each of these products, please see the most recently approved …
Outbreak Investigation of Listeria monocytogenes: Ready-to-Eat …
May 12, 2025 · The investigation was reopened in April 2025 after FDA investigators found Listeria in environmental samples collected from Fresh & Ready Foods, LLC during a routine …
Inspection Classification Database | FDA
The Food and Drug Administration (FDA) inspects and assesses regulated facilities to determine a firm's compliance with applicable laws and regulations, such as the Food, Drug, and …
List of Select Chemicals in the Food Supply Under FDA Review
On August 19, 2025, the U.S. Food and Drug Administration (FDA) updated this list of select chemicals currently under the agency’s review to provide more insight on the status of the …
FDA Issues Warning About Imported Cookware That May Leach …
Oct 15, 2025 · The U.S. Food and Drug Administration (FDA) is warning retailers and consumers not to sell or use certain imported cookware that may leach significant levels of lead (Pb) into …
FDA Clears First Blood Test Used in Diagnosing Alzheimer’s Disease
The FDA, an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary …
510 (k) Clearances | FDA
Section 510 (k) of the Food, Drug and Cosmetic Act requires device manufacturers who must register, to notify FDA of their intent to market a medical device at least 90 days in advance.