Device recall
Z-1510-2017: CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a…
FDA device recall · Class II · Ohmeda Medical
Key facts
| Recall number (Z-number) | Z-1510-2017 |
|---|---|
| Recall event | 76283 |
| Product | CarePlus Incubator Ohmeda-Ohio CarePlus Incubator- Incubators provide a controlled thermal environment for neonates who are unable to provide their own thermoregulation. They may also be used for short periods of time to facilitate the neonate s transition from the uterus to the external… |
| Product code | FMZ |
| Recalling firm | Ohmeda Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 13, 2018 |
| 510(k) numbers | K974349 |
| 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