Device recall
Z-1600-2023: Fisher Wallace Stimulator Models FW-100 and FW-200
FDA device recall · Class II · Fisher Wallace Laboratories Inc.
Key facts
| Recall number (Z-number) | Z-1600-2023 |
|---|---|
| Recall event | 91982 |
| Product | Fisher Wallace Stimulator Models FW-100 and FW-200 |
| Product code | QJQ |
| Recalling firm | Fisher Wallace Laboratories Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K903654 |
| FEI number | 3006258094 |
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