Recall Z-2089-2013— MCKESSON TECHNOLOGIES INC
Class II · Terminated
Class II FDA medical device recall by MCKESSON TECHNOLOGIES INC, initiated 2013-07-22, terminated 2014-06-19. FDA's recall record names no specific 510(k) clearance for this event. 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.. 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..
- Recalling firm
- MCKESSON TECHNOLOGIES INC
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-07-22
- Terminated
- 2014-06-19
- Firm location
- Alpharetta, GA, United States
Product description
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.
Reason for recall
The firm issued a clinical alert after users reported an issue where the Anesthesia-Rx system was interrupted ANF became temporarily unavailable during use.
Data sourced from openFDA. This site is unofficial and independent of the FDA.