Class II — Spectral Instruments Inc
| Recalling firm | Spectral Instruments Inc |
|---|---|
| Classification | Class II |
| Status | Ongoing |
| Reason | Momentary absence of On-Screen "X-Ray On" banner during run readiness check. |
| Product | Lago X |
| Quantity | 40 |
| Distribution | United States. |
| Initiated | 2026-07-24 |
| Classified | 2026-09-04 |
| Recall number | Z-2939-2026 |
| Initiation | FDA Mandated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Spectral Instruments Inc (Z-2939-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99631/
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