The intended use is to be paired with a weapon for aiming purposes.
Summary
The FDA issued a Class II for The intended use is to be paired with a weapon for aiming purposes. by Wilcox Industries Corp.. Reason: Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhancement to increase safety has been release.
Details
Source
Device Recall
External ID
Z-2675-2026
Action Date
2026-07-29
Status
Ongoing
Category
device
Product Description
The intended use is to be paired with a weapon for aiming purposes.
Lot/Code Info: None provided.
Quantity Affected: N/A
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.
Type: FDA Mandated
Recall Initiated: 2026-04-06
Company
Newington, NH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 154 device recalls issued in the same week, part of 373 device-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Wilcox Industries Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wilcox Industries Corp. have FDA actions?
This is the only FDA action we have on record for Wilcox Industries Corp. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-2675-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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