FDAFDA recall Z-2675-2026 · Jul 29, 2026
Wilcox Industries Corp.: The intended use is to be paired with a weapon for aiming purposes recall
Recall found
Product
The intended use is to be paired with a weapon for aiming purposes.
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.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- None provided.
- Quantity
- N/A
- Distribution
- US Nationwide distribution in the state of NH.
- Recalling firm
- Wilcox Industries Corp., Newington, NH
- Voluntary or mandated
- FDA Mandated
- Recall started
- 2026-04-06
Source: openFDA enforcement record Z-2675-2026 · search recall number Z-2675-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.