- Recalling firm
- Wilcox Industries Corp.
- 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.
- Affected products (lot / model / serial)
- None provided.
- Units affected
- N/A
- Distribution pattern
- US Nationwide distribution in the state of NH.
- Firm location
- Newington, NH, United States
- Recall type
- FDA Mandated
- How the firm notified customers
- N/A
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2675-2026
- Recall initiated
- April 6, 2026
- FDA classification date
- July 21, 2026
- FDA report date
- July 29, 2026
- FDA event ID
- 99059
- Last updated on HTM Vibe
- August 4, 2026