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Recall Observatory FDA recall evidence

Device product

Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that monitors and controls the dispensing of medications, narcotics and supplies during surgical procedures.

Z-2089-2013

July 22, 2013

Class II

Product summary

Firm
MCKESSON TECHNOLOGIES INC
Event
Event 65769
Status
Terminated
Classification
Class II
Quantity
106
Official record key
device-enforcement:Z-2089-2013

Official wording

Reason: The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.

Code information: Model Number (software version) 8.0.2 & 8.0.1 with RapiDispense

Distribution pattern: USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.