MCKESSON TECHNOLOGIES INC.: Medical Device Recall in 2014 - (Recall #: Z-1060-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class I

Date Initiated: March 15, 2013

Date Posted: March 12, 2014

Recall Number: Z-1060-2014

Event ID: 66287

Reason for Recall:

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.

Status: Terminated

Product Quantity: 10

Code Information:

MAC 14.3.1/MAC 14.3.1.1

Distribution Pattern:

Nationwide Distribution including CA, GA, IN, KY, MD, MI, OH, OK, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated