Z-2940-2026 Class II Ongoing
FDA device recall Z-2940-2026 was initiated by Spectral Instruments Inc on July 24, 2026 and is designated Class II. Reason for recall: Momentary absence of On-Screen "X-Ray On" banner during run readiness check. The recall status is ongoing. Affected quantity: 35.
Recall Details
- Product Type
- Devices
- Report Date
- August 26, 2026
- Initiation Date
- July 24, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 35
Product Description
Ami HTX
Reason for Recall
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Distribution Pattern
United States.
Code Information
All serial numbers.