Lago X — Class II medical device recall Z-2939-2026
Ongoing recall by Spectral Instruments Inc, reported 2026-08-26. Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
| Recall number | Z-2939-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Spectral Instruments Inc, Tucson, AZ, United States |
| Recall initiated | 2026-07-24 |
| Classified | 2026-09-04 |
| Reported by FDA | 2026-08-26 |
| Quantity | 40 |
Product
Lago X
Reason for recall
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2939-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.