Device recall
Z-1123-2009: Operon Electrical Operating Room Table. The device is used as an electrical…
FDA device recall · Class II · Berchtold Corp.
Key facts
| Recall number (Z-number) | Z-1123-2009 |
|---|---|
| Recall event | 51276 |
| Product | Operon Electrical Operating Room Table. The device is used as an electrical operating room table. |
| Product code | GDC |
| Recalling firm | Berchtold Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2009 |
| 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