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Open, Classified

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

FDA Recall Z-2675-2026 · Posted 2026-07-21

Recalling FirmWilcox Industries Corp.
Recall StatusOpen, Classified
Product CodeREU
Date Initiated2026-04-06

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.

Firm Action

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. Wilcox provided customers with contact information for our customer service as well to help facilitate returns and any questions. If this involved a medical device, has a Medical Device Report (MDR) been submitted to FDA?* Yes No N/A Unknown Other Important

Root Cause

Radiation Control for Health and Safety Act

Distribution Pattern

US Nationwide distribution in the state of NH.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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