Class II

Medical Device Recall: The intended use is to be paired with a weapon for aiming purposes.

Wilcox Industries Corp. · April 6, 2026

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.

States Affected

NATIONWIDE

Quantity Affected

N/A

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2675-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.