Wilcox Industries Corp. recalls The intended use is to be paired with a weapon for aiming purposes.

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.

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

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

• FDA enforcement recordOfficial FDA database entry for Z-2675-2026
• FDA device classification · REUOfficial FDA classification for this device type
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Wilcox Industries Corp.Search for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.