FDA recall record

Wilcox Industries The intended use is to be paired with a weapon for aiming purposes recall — FDA Z-2675-2026

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…

Class IIclassification
Z-2675-2026official record ID
Jul 29, 2026report date

Recall record at a glance

Official recordZ-2675-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmWilcox Industries Corp.
Report dateJul 29, 2026
Recall initiation dateApr 6, 2026
QuantityN/A
LocationNewington, NH, United States

Official product description

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

Why the product was recalled

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.

Distribution information

US Nationwide distribution in the state of NH.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: FDA Mandated. Initial notification: N/A.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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