Recall Z-2939-2026

Spectral Instruments Inc · initiated July 24, 2026

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Lago X

Codes / lots: All serial numbers.

Reason for recall

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

FDA-determined cause: Radiation Control for Health and Safety Act

Action taken

Customer notification letters dated August 21, 2023 and allows for scheduling of the software upgrade corrections.

Details

Recall number
Z-2939-2026
Initiated
July 24, 2026
Posted by FDA
August 14, 2026
Product code
RCE – Cabinet X-Ray, Industrial
Quantity
40
Distribution
United States.
Recalling firm
Spectral Instruments Inc, Tucson, AZ

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-2940-2026 Class IIAmi HTXMomentary absence of On-Screen "X-Ray On" banner during run readiness check. 07/24/2026Open, Classified