Device recall
Z-1060-2014: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a…
FDA device recall · Class I · MCKESSON TECHNOLOGIES INC.
Key facts
| Recall number (Z-number) | Z-1060-2014 |
|---|---|
| Recall event | 66287 |
| Product | McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment. The system provides… |
| Product code | BSZ |
| Recalling firm | MCKESSON TECHNOLOGIES INC. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 1, 2014 |
| 510(k) numbers | K113633 |
| FEI number | 3009662297 |
At a glance
- 1–9 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