Vycor Viewsite Brain Access System (VBAS): Class 1 Recall - Unidentified Fiber Found on Device
MedSun: Newsletter #81, February 2013

FDA MedWatch Safety Alert

Vycor Medical recalled its' VBAS because an unidentified black fiber was found on the device. Vycor Medical called their customers requesting that they place products of Model # TC171105, Lot # VM83450 into quarantine until further notice.

Additional Information:

FDA MedWatch Safety Alert. Vycor Viewsite Brain Access System (VBAS): Class 1 Recall - Unidentified Fiber Found on Device. January 30, 2013.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm337475.htm


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