Device recall
Z-2248-2017: Berchtold Chromophare F300 Exam Light CHROMOPHARE examination lights are medical…
FDA device recall · Class II · Stryker Communications
Key facts
| Recall number (Z-number) | Z-2248-2017 |
|---|---|
| Recall event | 77261 |
| Product | Berchtold Chromophare F300 Exam Light CHROMOPHARE examination lights are medical lights used for local illumination of the patients' body so that illnesses, injuries and disabilities can be diagnosed and treated |
| Product code | KZF |
| Recalling firm | Stryker Communications |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 20, 2017 |
| FEI number | 3002975342 |
At a glance
- None Linked 510(k)s
- 1–9 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