FDA Medical devices recall ·
The intended use is to be paired with a weapon for aiming purposes recall
- Recall number
- Z-2675-2026
- Date
- (initiated April 6, 2026)
- Company / brand
- Wilcox Industries Corp.
25 Piscataqua Dr, Newington, NH, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- N/A
- Hazard tags
- Software
- Initiated by
- FDA Mandated
Read the official FDA notice ↗
Product
The intended use is to be paired with a weapon for aiming purposes.
Why was it 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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
None provided.
Distribution
US Nationwide distribution in the state of NH.
States: New Hampshire
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2675-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.