Device recall
Z-2595-2016: Adult ThermoGard Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m)…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-2595-2016 |
|---|---|
| Recall event | 73607 |
| Product | Adult ThermoGard Dual Dispersive Electrodes (for patients >15 kg.), 10' (3.05m) Cable, Catalog Number 51-7310. Intended to be used for the dispersion and return to the electrosurgical generator. |
| Product code | GEI |
| Recalling firm | Conmed Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 24, 2018 |
| 510(k) numbers | K140658 |
| FEI number | 1317214 |
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