Device recall
Z-1488-2013: Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are…
FDA device recall · Class II · Berchtold Corp.
Key facts
| Recall number (Z-number) | Z-1488-2013 |
|---|---|
| Recall event | 65062 |
| Product | Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls are used to operate OPERON surgical tables |
| Product code | GDC |
| Recalling firm | Berchtold Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2017 |
| 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