Fresh Recalls

FDAClass II · Medical device · Recall Z-2675-2026 · Recalled July 29, 2026

The intended use is to be paired with a weapon for aiming purposes recall — Wilcox Industries Corp.

Agency report date: July 29, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
The intended use is to be paired with a weapon for aiming purposes
Company / brand
Wilcox Industries
Lot / serial / date codes
None provided.
Distribution
US Nationwide distribution in the state of NH.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: The intended use is to be paired with a weapon for aiming purposes

3. Open the official notice or contact

Official recall ID
Z-2675-2026
Brand
Wilcox Industries
Classification
Class II
Units affected
N/A
Recall status
Ongoing
Initiated
FDA Mandated

Affected products

Companies & origin

Recalling firm location
Newington, NH, United States
Firm address
25 Piscataqua Dr, N/A, 03801-7816

Identifying details (verbatim from the notice)

Product codes / lots
None provided.
Distribution
US Nationwide distribution in the state of NH.
Firm notified the public via
N/A
FDA event ID
99059
Recall initiated
April 6, 2026
FDA classified
July 21, 2026
FDA report date
July 29, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

Report a data error on this page