Class II
Medical Device Recall: Ami HTX
Spectral Instruments Inc · July 24, 2026
Reason for Recall
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Distribution
United States.
Quantity Affected
35
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2940-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.