May 08
Getinge/Maquet Cardiohelp System: Potential Insufficient Packaging Sterility with HLS Set Advanced - Letter to Health Care Providers
Medical Devices
FDA Commissioner Dr. Robert M. Califf discusses nutrition and offers a peek at some new packaging label prototypes.
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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.
Learn MoreMay 08
Medical Devices
May 08
Medical Devices, Radiation-Emitting Products
May 08
Medical Devices
The 50th biosimilar approval milestone also reflects our strategic approach to biosimilars, as outlined in the FDA’s Biosimilars Action Plan.
I recently had the privilege of official travel to the European Union with our global affairs team.
I recently had the privilege of official travel to the U.K. with our global affairs team.
FDA MedWatch Safety Information
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