Device recall
Z-0186-2010: XTEN DF cupola, P/N: 567800999. Intended to provide visible illumination for the…
FDA device recall · Class II · MAQUET Inc.
Key facts
| Recall number (Z-number) | Z-0186-2010 |
|---|---|
| Recall event | 53499 |
| Product | XTEN DF cupola, P/N: 567800999. Intended to provide visible illumination for the surgical field or for the examination of the patient. |
| Product code | FSY |
| Recalling firm | MAQUET Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2012 |
| 510(k) numbers | K040735 |
| FEI number | 3008355164 |
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