Device recall
Z-2406-2019: Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural…
FDA device recall · Class II · Ad-Tech Medical Instrument Corporation
Key facts
| Recall number (Z-number) | Z-2406-2019 |
|---|---|
| Recall event | 83179 |
| Product | Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes |
| Product code | GYC |
| Recalling firm | Ad-Tech Medical Instrument Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 20, 2023 |
| 510(k) numbers | K053363 |
| FEI number | 2183456 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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