Cordis Yanks Catheters Over Potentially Fatal Flaw
The worldwide recall, issued Jan. 14 but made public by the U.S. Food and Drug Administration on Friday, affects Cordis’ Fire Star Rx and Dura Star Rx PTCA balloon catheters, which do not deflate properly and could potentially cause fatal injuries, the agency said.
The recall has been deemed a Class I recall, which is the most serious...
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