Recall Z-2089-2013 ยท BRY Cabinet, Table And Tray, Anesthesia
MCKESSON TECHNOLOGIES INC
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.
| Date | Aug 26, 2013 (initiated Jul 22, 2013) |
| Status | Terminated |
| 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. |
| Root cause | Software design |
| Action | McKesson sent a Clinical Alert letter dated July 22, 2013 to all affected customers. The letter identified the affected product, symptoms, and actions to be taken. McKesson committed to releasing 8.0.2 Update 1.5 to affected customers which will include enhanced code to prevent the unhandled excpetion errors. Additional resolution steps were included in the letter. For questions call 1-800-700-8737. |
| Quantity | 106 |
| Distribution | USA Nationwide Distribution in the states AR, MD, NJ, NY, PA, and WV. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.