# FDA recall Z-2939-2026

> **Spectral Instruments Inc** · Class II · device recall initiated 2026-07-24.

## Product

Lago X

## Reason for recall

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

## Distribution

United States.

## Key facts

- **Recall number:** Z-2939-2026
- **Recalling firm:** Spectral Instruments Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-07-24
- **Report date:** 2026-08-26

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Tucson, AZ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2939-2026

## Citation

> MORVS. FDA recall Z-2939-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2939-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*