Device recall
Z-2089-2013: Mc Kesson Anesthesia-Rx Model Number 8.0.2 & 8.0.1 with RapiDispense Product…
FDA device recall · Class II · MCKESSON TECHNOLOGIES INC
Key facts
| Recall number (Z-number) | Z-2089-2013 |
|---|---|
| Recall event | 65769 |
| 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. |
| Product code | BRY |
| Recalling firm | MCKESSON TECHNOLOGIES INC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 19, 2014 |
| FEI number | 3003781505 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database