CONSTELLATION Vision System - Recall
MedSun: Newsletter #51, August 2010

FDA MedWatch Safety Alert

Alcon initiated the recall after it identified both software and hardware problems which have been associated with unexpected system loss of power (shutdowns), unintended system error messages, unresponsive touchscreens, and system setting and infusion performance problems. These events may cause eye injuries, including blindness.

Additional Information:

FDA MedWatch Safety Alert. CONSTELLATION Vision System – Recall. July 20, 2010.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm219665.htm


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