Device recall
Z-0305-2009: Giraffe OmniBed, labeled in part: ***GE Healthcare 8880 Gorman Road Laurel, MD…
FDA device recall · Class II · Datex Ohmeda, Inc. dba GE Healthcare
Key facts
| Recall number (Z-number) | Z-0305-2009 |
|---|---|
| Recall event | 49097 |
| Product | Giraffe OmniBed, labeled in part: ***GE Healthcare 8880 Gorman Road Laurel, MD 20723 U.S.A. www.gehealthcare.com***. 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… |
| Product code | FMZ |
| Recalling firm | Datex Ohmeda, Inc. dba GE Healthcare |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 24, 2010 |
| FEI number | 1121732 |
At a glance
- None 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