Medical device recalls Moderate risk

Fisher Wallace Stimulator Models FW-100 and FW-200 recalled over fire hazard

Recall date
April 6, 2023
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Official notice title
Fisher Wallace Laboratories Inc. recalls Fisher Wallace Stimulator Models FW-100 and FW-200
Recall number
Z-1600-2023
FDA classification
Class II
Brand / firm
Fisher Wallace Laboratories Inc.
Sold / distributed
US Nationwide. Global Distribution.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Fisher Wallace Stimulator Models FW-100 and FW-200

Get recall alerts

Free email alert whenever Fisher Wallace Laboratories Inc. has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Fisher Wallace Laboratories Inc.