- Recalling firm
- Spectral Instruments Inc
- Reason for recall
- Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
- Affected products (lot / model / serial)
- All serial numbers.
- Units affected
- 35
- Distribution pattern
- United States.
- Firm location
- Tucson, AZ, United States
- Recall type
- FDA Mandated
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2940-2026
- Recall initiated
- July 24, 2026
- FDA classification date
- September 4, 2026
- FDA report date
- August 26, 2026
- FDA event ID
- 99631
- Last updated on HTM Vibe
- September 8, 2026