Fisher Wallace Stimulator Models FW-100 and FW-200

Recall Insight

This FDA Devices action (record #Z-1600-2023) was formally reported on May 24, 2023, with the manufacturer initiating the action on April 6, 2023. It is classified under Moderate severity (Class II), with a current status of Ongoing. Fisher Wallace Laboratories Inc. is listed as the recalling firm, operating out of Brooklyn, NY. Federal records indicate 43,489 total devices units are affected.

The documented reason for this recall is: 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 data in the federal record shows the product reached: US Nationwide. Global Distribution.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 3 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.