FDA recall Z-2675-2026

Wilcox Industries Corp. · Class II · device

Product

The intended use is to be paired with a weapon for aiming purposes.

Reason for recall

Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been released and all units should be returned to implement this change.

Distribution

US Nationwide distribution in the state of NH.

Key facts

Status
Ongoing
Initiation date
2026-04-06
Report date
2026-07-29
Voluntary/Mandated
FDA Mandated
Location
Newington, NH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2675-2026