Device recall
Z-1365-2011: ConMed System 2450 Electrosurgical Generator, REF 60-2450-230, 230V-240V, ConMed…
FDA device recall · Class II · ConMed Electrosurgery
Key facts
| Recall number (Z-number) | Z-1365-2011 |
|---|---|
| Recall event | 57544 |
| Product | ConMed System 2450 Electrosurgical Generator, REF 60-2450-230, 230V-240V, ConMed Electrosurgery, Centennial, CO. A general-purpose electrosurgical generator used in conjunction with an electrosurgical accessory handpiece for delivery of high (HF) electrosurgical current through an accessory… |
| Product code | GEI |
| Recalling firm | ConMed Electrosurgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 1, 2011 |
| 510(k) numbers | K052009 |
| FEI number | 3004491689 |
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