Recalled Medical Devices Received Fast-Track FDA Approval

Recalled Medical Devices Received Fast-Track FDA ApprovalA recently recalled medical device, the Axxent FlexiShield Mini, was originally approved by the U.S. Food and Drug Administration's 510(K) process.

NEW YORK, NY, May 04, 2011 /24-7PressRelease/ -- Patients are at risk of life-threatening injuries from a device meant to protect healthy tissue from unwanted radiation during cancer treatment. The medical device, called the Axxent FlexiShield Mini, has been classified

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