# FDA recall Z-2675-2026

> **Wilcox Industries Corp.** · Class II · device recall initiated 2026-04-06.

## 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.

## Distribution

US Nationwide distribution in the state of NH.

## Key facts

- **Recall number:** Z-2675-2026
- **Recalling firm:** Wilcox Industries Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-06
- **Report date:** 2026-07-29

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Newington, NH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2675-2026

## Citation

> AI Analytics. FDA recall Z-2675-2026. Retrieved 2026-09-01 from https://api.ai-analytics.org/recall/Z-2675-2026. Source: US FDA. Licensed CC0.

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