Device recall
Z-1047-05: Ohmeda Medical''s Giraffe OmniBeds and Giraffe Incubators
FDA device recall · Class II · Ohmeda Medical, A division of Datex-Ohmeda, Inc.
Key facts
| Recall number (Z-number) | Z-1047-05 |
|---|---|
| Recall event | 31665 |
| Product | Ohmeda Medical''s Giraffe OmniBeds and Giraffe Incubators |
| Product code | FMZ |
| Recalling firm | Ohmeda Medical, A division of Datex-Ohmeda, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 11, 2007 |
| 510(k) numbers | K010222, K020547, K993407 |
| FEI number | 1121732 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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