Device recall
Z-1508-2017: Giraffe Bedded Warmer, Panda Warmer Modifiction to Giraffe and Panda Warmer…
FDA device recall · Class II · Ohmeda Medical
Key facts
| Recall number (Z-number) | Z-1508-2017 |
|---|---|
| Recall event | 76283 |
| Product | Giraffe Bedded Warmer, Panda Warmer Modifiction to Giraffe and Panda Warmer- Infant radiant warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own physiology. Infant radiant warmers may be used to facilitate the neonate's transition to… |
| Product code | FMT |
| Recalling firm | Ohmeda Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 13, 2018 |
| 510(k) numbers | K090697 |
| FEI number | 1121732 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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