Class II — Fisher Wallace Laboratories Inc.
| Recalling firm | FISHER-WALLACE LABORATORIES Inc |
|---|---|
| Registered facility | FISHER WALLACE LABORATORIES Inc (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device. |
| Product | Fisher Wallace Stimulator Models FW-100 and FW-200 |
| Quantity | 43,489 total devices |
| Distribution | US Nationwide. Global Distribution. |
| Initiated | 2023-04-06 |
| Classified | 2023-05-17 |
| Recall number | Z-1600-2023 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Fisher Wallace Laboratories Inc. (Z-1600-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91982/
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