Device recall
Z-1565-2010: ConMed Goldline Hand Controlled With Blade Electrode, Rocker Switch, Safety…
FDA device recall · Class II · ConMed Electrosurgery
Key facts
| Recall number (Z-number) | Z-1565-2010 |
|---|---|
| Recall event | 55189 |
| Product | ConMed Goldline Hand Controlled With Blade Electrode, Rocker Switch, Safety Holster and 10 FT Cable, REF 130319A, Sterile R, Assembled in Mexico, ConMed Corporation, 525 French Rd., Utica, NY 13502. |
| Product code | GEI |
| Recalling firm | ConMed Electrosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2010 |
| 510(k) numbers | K791137 |
| FEI number | 3004491689 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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