Beckman Coulter UniCel DxC Synchron Clinical System - Ion Selective Electrode Flow Cell: Class I Recall
MedSun: Newsletter #47, April 2010

FDA MedWatch Safety Alert

FDA notified healthcare professionals of the Class I recall of UniCel DxC Synchron Clinical System - Ion Selective Electrode (ISE) Flow Cell. There may be excessive build-up of protein, bacteria, and sample tube additives in the instrument's ion selective electrode flow cell which may cause incorrect sodium results.

Additional Information:

FDA MedWatch Safety Alert. Beckman Coulter UniCel DxC Synchron Clinical System – Ion Selective Electrode Flow Cell: Class I Recall. March 11, 2010.
http://www.fda.gov/Safety/MedWatch/SafetyInformation/SafetyAlertsforHumanMedicalProducts/ucm204106.htm


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