FDA Devices recall · Reported July 29, 2026
The intended use is to be paired with a weapon for aiming purposes.
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 ret…
Wilcox Industries Corp. recalled The intended use is to be paired with a weapon for aiming purposes. - a moderate-severity action.
The intended use is to be paired with a weapon for aiming purposes. was recalled by Wilcox Industries Corp. in July 29, 2026. Reason: Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhanc…. Check the official notice for the remedy. Verify recall #Z-2675-2026 with the FDA Devices before acting.
The recall
Wilcox Industries Corp. issued this moderate-severity FDA Devices recall-Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhanc….
- Moderate
- severity level
- Class II
- classification
- July 29, 2026
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2675-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2675-2026) was formally reported on July 29, 2026, with the manufacturer initiating the action on April 6, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. Wilcox Industries Corp. is listed as the recalling firm, operating out of Newington, NH. Federal records list the affected scope as N/A.
The documented reason for this recall is: 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 data in the federal record shows the product reached: US Nationwide distribution in the state of NH.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,861 medical devices recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | Z-2675-2026 |
| Date reported | July 29, 2026 |
| Date initiated | April 6, 2026 |
| Recalling firm | Wilcox Industries Corp. |
| Firm location | Newington, NH |
| Affected scope | N/A |
| Distribution | US Nationwide distribution in the state of NH. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2675-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Methodology · Corrections · Archive as of August 2026