FDA recall Z-2940-2026
Spectral Instruments Inc · Class II · device
Product
Ami HTX
Reason for recall
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Distribution
United States.
Key facts
- Status
- Ongoing
- Initiation date
- 2026-07-24
- Report date
- 2026-08-26
- Voluntary/Mandated
- FDA Mandated
- Location
- Tucson, AZ, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2940-2026