The U.S. Food and Drug Administration (FDA) posted a medical device safety alert concerning McKesson Anesthesia Care System with code number MAC 14.3.1/MAC 14.3.1.1.
There was an occurrence where the patient case data did not match the patient data when the case was recalled in the Anesthesia Care Record in that it included data from another case.
For details, please refer to the FDA website:
http://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?action=select&recall_number=Z-1060-2014&w=03122014&lang=eng
If you are in possession of the affected product, please contact your supplier for necessary actions.
Posted on 13 March 2014