Improvements made to FDA medical device recall databases

Improvements to public databases are expected to increase and improve access to safety information on marketed medical devices, according to a press release from the U.S. Food and Drug Administration’s Center for Devices and Radiological Health.The 510(k) and premarket approval databases will now feature a Center for Devices and Radiological Health recalls hyperlink at the bottom of a record if there are recalls associated with that medical device.

Full Story →