← FDA ENFORCEMENT
Z-2939-2026Class II
Spectral Instruments Inc
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
Spectral Instruments Inc
Product type
Device
Status
Ongoing
Report date
2026-08-26
Distribution
United States.
Firm state
AZ
Product quantity
40
Initiated by
FDA Mandated
Reason for recall
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Product description
Lago X
Code / lot info
All serial numbers.
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →