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MCKESSON TECHNOLOGIES INC recalls Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product Usage: Automated anesthesia cart that
Recalled September 4, 2013 · FDA recall Z-2089-2013 · MCKESSON TECHNOLOGIES
Hazard
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use. · FDA Class II
Units
106
Sold at
USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV.
Description
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.
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.
Manufacturer(s)
MCKESSON TECHNOLOGIES INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →