Data Foundry

Medical device recalls 2026

The intended use is to be paired with a weapon for aiming purposes — Class II medical device recall Z-2675-2026

Ongoing recall by Wilcox Industries Corp., reported 2026-07-29, distributed nationwide. Wilcox is notifying all customers who have purchased a product from the BOSS Xe family that a software enhance

Recall numberZ-2675-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedFDA mandated
Recalling firmWilcox Industries Corp., Newington, NH, United States
Recall initiated2026-04-06
Classified2026-07-21
Reported by FDA2026-07-29
DistributedNationwide (US)
Reason classessoftware

Product

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2675-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.