Wilcox BOSS Xe Family
The BOSS Xe family has a software enhancement to increase safety and all units should be returned.
Moderate risk
Using it may cause temporary or medically reversible health problems. Serious harm is unlikely.
FDA Class II recall · How risk is rated
What happened
Wilcox Industries Corp., of Newington, New Hampshire, notified customers who 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 company began the recall on April 6, 2026, and the FDA added it to the Enforcement Report on July 21, 2026. Distribution was in the state of New Hampshire.
Summary by Recall Canary from the FDA notice.
What to do
If you have this product:
- 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.
Is yours affected?
Compare these product details with yours, then check the recall notice for any restrictions.
The intended use is to be paired with a weapon for aiming purposes.
Details
- Company began the recall
- Sold in
US Nationwide distribution in the state of New Hampshire.
- Event ID
- 99059
- Recall No.
- Z-2675-2026
- Company
- Wilcox Industries Corp.Newington, New Hampshire
- Hazard
- Software defect
- Recall type
- FDA Mandated
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
