Recall Z-2939-2026— Spectral Instruments Inc
Class II · Ongoing
Class II FDA medical device recall by Spectral Instruments Inc, initiated 2026-07-24. FDA's recall record names no specific 510(k) clearance for this event. Product: Lago X. Reason: Momentary absence of On-Screen "X-Ray On" banner during run readiness check..
- Recalling firm
- Spectral Instruments Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-07-24
- Firm location
- Tucson, AZ, United States
Product description
Lago X
Reason for recall
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Data sourced from openFDA. This site is unofficial and independent of the FDA.