Dec 20
2024 Medical Device Recalls
Medical Devices, Radiation-Emitting Products
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
December 4, 2024 - Clinicians hear directly from the CDC, FDA, HHS, and NIH about what we can do to address the recent surge in syphilis and its impact on individuals, pregnant people and babies.
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Health professionals, consumers and patients can voluntarily report observed or suspected adverse events for human medical products to FDA. Voluntary reporting can help FDA identify unknown risk for approved medical products.
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Medical Devices, Radiation-Emitting Products
Dec 20
Medical Devices
Dec 11
Medical Devices
FDA’s ongoing efforts serve to make tobacco-related disease and death part of our nation’s past, ensuring a healthier future for our youth.
OCI investigators have been conducting and coordinating criminal investigations of suspected illegal activities involving FDA-regulated products.
FDA collaborates with stakeholders across disciplines and sectors to promote the health of humans, animals, and the environment.
FDA MedWatch Safety Information
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