Z-2675-2026 Class II Ongoing
FDA device recall Z-2675-2026 was initiated by Wilcox Industries Corp. on April 6, 2026 and is designated Class II. 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 th… The recall status is ongoing. Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- July 29, 2026
- Initiation Date
- April 6, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- N/A
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.
Distribution Pattern
US Nationwide distribution in the state of NH.
Code Information
None provided.