Apr 15
Recall of Certain Saline and Sterile Water Medical Products Associated with Nurse Assist: FDA Safety Communication
Medical Devices
Health Professionals
FDA Collaborates with Health Professional Societies, Trade Associations, and Academia
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FDA Commissioner Dr. Robert Califf Discusses Nutrition Labeling on Food Packages - March 13, 2024
Call-To-Action Title
FDA Commissioner Dr. Robert Califf Discusses Nutrition Labeling on Food Packages - March 13, 2024
FDA Commissioner Dr. Robert M. Califf discusses nutrition and offers a peek at some new packaging label prototypes.
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How to Report Adverse Events to FDA MedWatch
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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Apr 15
2024 Medical Device Recalls
Medical Devices, Radiation-Emitting Products
Apr 15
Abbott/Thoratec Corp. Recalls HeartMate II and HeartMate 3 Left Ventricular Assist System (LVAS) due to Long-term Buildup Causing an Obstruction
Medical Devices
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FDA VOICES: PERSPECTIVES FROM FDA EXPERTS
Reflections on Travel to Europe – Part One
I recently had the privilege of official travel to the U.K. and European Union with our global affairs team.
Harnessing the Potential of Artificial Intelligence
At the FDA, we’ve been working for years to anticipate and prepare for the challenges of Artificial Intelligence (AI), and also to harness its potential.
FDA Works to Make Informed Consent Easier to Understand
FDA and the Office for Human Research Protections have published a draft guidance: “Key Information and Facilitating Understanding in Informed Consent.”
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Stakeholder Engagement Staff
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Food and Drug Administration
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Silver Spring, MD 20993
United States
Office of External Affairs
Office of the Commissioner
Food and Drug Administration
10903 New Hampshire Ave WO32-5367
Silver Spring, MD 20993
United States
Director, Dayle Lewis Cristinzio
202-430-9745
Hours Available
Stakeholder Engagement Staff
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