
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 …
Drugs | FDA
FDA uses science and data to ensure that approved drugs are of a high quality, safe, and effective. Learn more about the FDA’s role in reviewing, approving, and monitoring drugs in …
Recalls, Market Withdrawals, & Safety Alerts | FDA
Recalls, Market Withdrawals, & Safety Alerts The list below provides information gathered from press releases and other public notices about certain recalls of FDA-regulated products.
Warning Letters | FDA
To obtain additional available information, contact FDA. Requests to FDA for agency records should be sent to: Food and Drug Administration Division of Freedom of Information (HFI-35), …
FDA Newsroom | FDA
The latest news and events at the U.S. Food and Drug Administration (FDA) and resources for journalists.
FDA Dashboards - Inspections
FDA does not issue CGMP certificates at the conclusion of an inspection. Instead, this dashboard provides the outcomes, including classification and other details, of a firm’s most recent …
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 …
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 …
Outbreak Investigation of Salmonella: Cucumbers (May 2025) | FDA
Jun 30, 2025 · The FDA and CDC, in collaboration with state and local partners, investigated illnesses in a multistate outbreak of Salmonella Montevideo infections linked to cucumbers …
Drugs@FDA - Food and Drug Administration
Drugs@FDA includes most of the drug products approved since 1939. The majority of patient information, labels, approval letters, reviews, and other information are available for drug …