Device recall
Z-0873-2007: Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite…
FDA device recall · Class II · Vision Systems Group, A Div of Viking Systems
Key facts
| Recall number (Z-number) | Z-0873-2007 |
|---|---|
| Recall event | 37793 |
| Product | Light Source 300 Watt Xenon Lamp used in the following models: Viking EndoSite Xenon, Model 8050-1 and Boston Scientific Spyglass 300W Light Source (M00546190) |
| Product code | KOG |
| Recalling firm | Vision Systems Group, A Div of Viking Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2007 |
| 510(k) numbers | K864385 |
| FEI number | 1000305720 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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