FDA Medical Device Recalls (openFDA)
Wilcox Industries Corp.: The intended use is to be paired with a weapon for aiming purposes.
- Recall number
- Z-2675-2026
- Recalling firm
- Wilcox Industries Corp.
- Product
- The intended use is to be paired with a weapon for aiming purposes.
- Status
- Open, Classified
- Initiated
- 2026-04-06
- Posted
- 2026-07-21
- Terminated
- not on file
- 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 released and all units should be returned to implement this change.
- Root cause
- Radiation Control for Health and Safety Act
- Action
- 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. Wilcox provided customers with contact information for our customer service as well to help facilitate returns and any questions. If this involved a medical device, has a Medical Device Report (MDR) been submitted to FDA?* Yes No N/A Unknown Other Important
- Quantity
- not on file
- Distribution
- US Nationwide distribution in the state of NH.
- Lot, serial or model codes
- None provided.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- REU
- Firm FEI
- 3007858386
- Firm city
- Newington
- Firm state
- NH
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28