- 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 ensuring the
- 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
- Contact FDA | FDA
By phone: Call 1-888-INFO-FDA (1-888-463-6332) Call the FDA Consumer Complaint Coordinator for your state or region For more details, see How to Report a Problem
- Novel Drug Approvals for 2025 | FDA
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 Prescribing Information (or
- Drug Approvals and Databases | FDA
Novel Drugs at FDA: CDER’s New Molecular Entities and New Therapeutic Biological Products Drug and Biologic Approval and IND Activity Reports This Week's Drug Approvals Drug Trials Snapshots
- 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
- 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 drugs, vaccines
- FDA Adverse Event Reporting System (FAERS) Database
FDA Adverse Event Reporting System Database supports the FDA's post-marketing safety surveillance program for all marketed drug and therapeutic biologic products
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