FDAFDA · Food and drugs·Recall number Z-2675-2026
The intended use is to be paired with a weapon for aiming purposes.
Published July 29, 2026 · Recall initiated: April 6, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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 Mandated
Recall details
- Manufacturer
- Wilcox Industries Corp.
- Distributor
- US Nationwide distribution in the state of NH.
- Lot
- None provided.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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