Device recall
Z-0474-2023: Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction…
FDA device recall · Class II · ConMed Corporation
Key facts
| Recall number (Z-number) | Z-0474-2023 |
|---|---|
| Recall event | 91165 |
| Product | Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187 |
| Product code | GEI |
| Recalling firm | ConMed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 13, 2026 |
| 510(k) numbers | K033003 |
| FEI number | 3001451571 |
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