Device recall
Z-2168-2013: OPERON D850 Surgical Table Product Usage: Surgical Table
FDA device recall · Class II · Berchtold Corp.
Key facts
| Recall number (Z-number) | Z-2168-2013 |
|---|---|
| Recall event | 65960 |
| Product | OPERON D850 Surgical Table Product Usage: Surgical Table |
| Product code | GDC |
| Recalling firm | Berchtold Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 10, 2013 |
| FEI number | 1220685 |
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