Spectral Instruments Inc recall Z-2939-2026 · FDA Recalls

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Class IIDeviceOngoing

Spectral Instruments Inc

Lago X

Reason for recall

Momentary absence of On-Screen "X-Ray On" banner during run readiness check.

Details

Recall number: Z-2939-2026
Event ID: 99631
Recall initiated: Jul 24, 2026
Classified: Sep 4, 2026
Reported: Aug 26, 2026
Quantity: 40
Distribution: United States.
Initiated by: FDA Mandated
Firm location: Tucson, AZ, United States
Lot / code info: All serial numbers.