Medical Device Safety and Recalls: FDA Announces Improvements To The Medical Device Recalls Database

["U.S. Food & Drug Administration (FDA)" <fda@xxxxxxxxxxxxxxxxxxxxxxx>]

Title: Medical Device Safety and Recalls: FDA Announces Improvements To The Medical Device Recalls Database

The Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH) is pleased to announce improvements to several public databases that will increase access to safety information on marketed medical devices. The improvements include adding new fields to the Medical Device Recalls database and providing links to the recall database from FDA’s 510(k)Premarket Notification and Premarket Approval (PMA) database.

Read more about the improvements.

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