Device recall
Z-0288-04: Radiant Heater Door Vent for Ohmeda Medical''s Giraffe (tm) OmniBed neonate bed.
FDA device recall · Class II · Ohmeda Medical, A Div of Datex-Ohmeda, Inc
Key facts
| Recall number (Z-number) | Z-0288-04 |
|---|---|
| Recall event | 27490 |
| Product | Radiant Heater Door Vent for Ohmeda Medical''s Giraffe (tm) OmniBed neonate bed. |
| Product code | FMZ |
| Recalling firm | Ohmeda Medical, A Div of Datex-Ohmeda , Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 11, 2005 |
| 510(k) numbers | K020543 |
| 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