Device recall
Z-2598-2016: Adult Dual Dispersive Electrodes (for patients >15 kg.), use with the Birtcher…
FDA device recall · Class II · Conmed Corporation
Key facts
| Recall number (Z-number) | Z-2598-2016 |
|---|---|
| Recall event | 73607 |
| Product | Adult Dual Dispersive Electrodes (for patients >15 kg.), use with the Birtcher Pad Sensing System (PSS) on the Birtcher Systems 6000, 6400, 6500 and CONMED Systems 7500 and 7550 ABC generators or conventional electrosurgery units with similar contact monitoring systems, 10' (3.05m) Cable, Catalog… |
| 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