The cases in the literature article performed between february 2006 and october 2011; the exact date of the event being reported in unknown.The subject device was not returned; therefore, physical analysis cannot be performed.There is no indication that the reported event is related to product specifications nonconformance or misuse.However, transient ischemic attack is a known risk associated with endovascular procedures and are listed as such in the direction¿s for use (dfu).Therefore, a root cause of anticipated procedural complication has been assigned to this event.Device was not returned to manufacturer.
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