Device recall
Z-0039-06: Datex-Ohmeda Aespire Carestation. This device is not marketed in the US.
FDA device recall · Class II · Datex-Ohmeda Inc
Key facts
| Recall number (Z-number) | Z-0039-06 |
|---|---|
| Recall event | 33678 |
| Product | Datex-Ohmeda Aespire Carestation. This device is not marketed in the US. |
| Product code | BSZ |
| Recalling firm | Datex-Ohmeda Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 1, 2007 |
| FEI number | 2183066 |
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