# FDA recall Z-1600-2023

> **Fisher Wallace Laboratories Inc.** · Class II · device recall initiated 2023-04-06.

## Product

Fisher Wallace Stimulator Models FW-100 and FW-200

## Reason for recall

If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device.

## Distribution

US Nationwide. Global Distribution.

## Key facts

- **Recall number:** Z-1600-2023
- **Recalling firm:** Fisher Wallace Laboratories Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-06
- **Report date:** 2023-05-24

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brooklyn, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1600-2023

## Citation

> AI Analytics. FDA recall Z-1600-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1600-2023. Source: US FDA. Licensed CC0.

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