Device recall
Z-0041-2020: Giraffe Omnibed - Product Usage: The OmniBed is a combination of an infant…
FDA device recall · Class II · Ohmeda Medical
Key facts
| Recall number (Z-number) | Z-0041-2020 |
|---|---|
| Recall event | 81419 |
| Product | Giraffe Omnibed - Product Usage: The OmniBed is a combination of an infant incubator and an infant warmer. The device can be operated as an incubator or as a warmer and can transition from one mode to the other on user s demand. It cannot be operated in both modes at the same time. Incubators and… |
| Product code | FMZ |
| Recalling firm | Ohmeda Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 2, 2020 |
| 510(k) numbers | 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