Fisher Wallace recalls two stimulator models due to overheating risk from incorrect battery installation, potentially causing burns. Affected units have specific serial numbers and UDI-DI codes.
If the batteries are installed incorrectly, the product may overheat, possibly leading to pain, discomfort, irritation, or even burns during use of the device.
Fisher Wallace is recalling their FW-100 and FW-200 stimulator models because incorrect battery installation can cause overheating, leading to pain, discomfort, irritation, or burns. This risk affects users who have installed batteries improperly.
The device may overheat if batteries are installed incorrectly, which can cause pain, discomfort, irritation, or burns during use. This happens because the battery configuration affects the device's electrical safety.
Users of Fisher Wallace Stimulator Models FW-100 and FW-200 are affected. Those who have installed batteries incorrectly are at higher risk of overheating and potential burns.
Check for the model number on your device (FW-100 or FW-200). Look for the UDI-DI code 00860000919005 for FW-100 or 00860000919012 for FW-200. Serial numbers range from 2020200000 to 2022278000 for FW-100 and 2021140129T to 2022030528T for FW-200.
Ensure batteries are installed correctly according to the device's instructions to prevent overheating.
Fisher Wallace Stimulator Models FW-100 and FW-200.
Check for the model number (FW-100 or FW-200) and look for the UDI-DI code 00860000919005 for FW-100 or 00860000919012 for FW-200. Serial numbers range from 2020200000 to 2022278000 for FW-100 and 2021140129T to 2022030528T for FW-200.
Ensure batteries are installed correctly to prevent overheating. The recall does not require discarding or returning the device.
We’ve drafted a message you can send Fisher Wallace to request your refund or repair — edit it as you like.
Subject: Recall Z-1600-2023 — Fisher Wallace Fisher Wallace Hello, I own a Fisher Wallace that is covered by recall Z-1600-2023 from Fisher Wallace. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
