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MCKESSON TECHNOLOGIES INC. recalls McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collect
Recalled March 12, 2014 · FDA recall Z-1060-2014 · MCKESSON TECHNOLOGIES
Hazard
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 (ACR) in that it included data from another case. · FDA Class I
Units
10
Sold at
Nationwide Distribution including CA, GA, IN, KY, MD, MI, OH, OK, and WA.
Description
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 (ACR) in that it included data from another case.
Product
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides clinical decision support by communicating potential Adverse Drug Event alerts proactively during the pre-anesthesia evaluation and at the point-of-care. The system is generally indicated in the anesthetizing environment when the anesthesia provider decides to perform a patient assessment, to generate a paper and/or electronic record of the administration of anesthesia to a patient, and to document care.
Manufacturer(s)
MCKESSON TECHNOLOGIES INC.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →