Spectral Instruments recalls Lago X devices due to potential momentary absence of X-Ray On banner during run readiness check. No specific remedy provided in recall notice.
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Spectral Instruments is recalling all Lago X devices because they may show a momentary absence of the X-Ray On banner during run readiness checks. This could affect the device's safety features but does not cause immediate harm.
The device may briefly fail to display the X-Ray On banner during run readiness checks. This could lead to users not knowing when the X-Ray feature is active, potentially causing safety issues if the feature is critical for their use.
All owners of Lago X devices are affected. Users who rely on the X-Ray feature for safety are most at risk.
Check for Lago X devices with any serial number. The recall applies to all units produced by Spectral Instruments.
Verify if the X-Ray On banner appears during run readiness checks.
The recall does not require stopping use; the hazard is low risk and does not cause immediate harm.
No remedy is provided in the recall notice.
All Lago X devices with any serial number are affected by this recall.
We’ve drafted a message you can send Spectral Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-2939-2026 — Spectral Instruments Spectral Instruments Hello, I own a Spectral Instruments that is covered by recall Z-2939-2026 from Spectral Instruments. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
