ClearanceBrief
Recall Z-2675-2026 ยท REU Laser Aiming Product, Visible

Wilcox Industries Corp.

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

DateJul 21, 2026 (initiated Apr 6, 2026)
StatusOpen, Classified
ReasonWilcox 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.
Root causeRadiation Control for Health and Safety Act
ActionWilcox 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
DistributionUS Nationwide distribution in the state of NH.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.