Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system Recalled by MCKESSON TECHNOLOGIES INC. Due to There was an occurrence where the patient case...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MCKESSON TECHNOLOGIES INC. directly.
Affected Products
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.
Quantity: 10
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MCKESSON TECHNOLOGIES INC.
MCKESSON TECHNOLOGIES INC. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report