Recalled Medical Devices Received Fast-Track FDA Approval
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 as the most serious type of recall.
According to the U.S. Food and Drug Administration (FDA), recalls of this level involve "situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death."
"Unsurprisingly, the shield was approved by the FDA via an abbreviated ...




