Wilcox Industries Corp. recalls The intended use is to be paired with a weapon for aiming purposes.
- Recalling company
- Wilcox Industries Corp.
- Product
- The intended use is to be paired with a weapon for aiming purposes.
- Reason
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 6, 2026
- Reported
- Jul 29, 2026
- Distribution
- US Nationwide distribution in the state of NH.
- Status
- Ongoing
- Quantity
- N/A
- Lot / codes
- None provided.
- Company location
- Newington, NH
- Recall type
- FDA Mandated
- Recall number
- Z-2675-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2675-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.