Device recall
Z-1501-2017: Giraffe Exam Light The Exam Light illuminates body surfaces and facilitates…
FDA device recall · Class II · Ohmeda Medical
Key facts
| Recall number (Z-number) | Z-1501-2017 |
|---|---|
| Recall event | 76283 |
| Product | Giraffe Exam Light The Exam Light illuminates body surfaces and facilitates patient observation during a medical examination. It increases ambient light to facilitate performance of procedures on the mattress field. It is designed to mount on the accessory railings of the Giraffe OmniBed, incubators… |
| Product code | KZF |
| Recalling firm | Ohmeda Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 13, 2018 |
| FEI number | 1121732 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 1–9 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