Most Medical Devices Recalled By the FDA Because of Serious Risks Did Not Undergo Clinical Trials

ScienceDaily (Feb. 28, 2011) — Most medical devices recently recalled by the Food and Drug Administration because of very serious risks were initially approved through an expedited process or were exempt from regulatory review, according to a report posted online February 14 that will be published in the June 14 print issue of Archives of Internal Medicine.

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