Fisher Wallace Stimulator recall
Fisher Wallace Stimulator Models FW-100 and FW-200
Why was Fisher Wallace Stimulator 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.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
FW-100: UDI-DI 00860000919005, Serial Numbers 2020200000-2022278000; FW-200: UDI-DI 00860000919012, Serial Numbers 2021140129T-2022030528T
- Product
- Fisher Wallace Stimulator Models FW-100 and FW-200
- Recalling firm
- Fisher Wallace Laboratories Inc.
- Quantity
- 43,489 total devices
- Distribution
- US Nationwide. Global Distribution.
- Recall date
- May 24, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)