Spectral Instruments recalls Ami HTX devices due to potential momentary absence of X-Ray On banner during run readiness checks. No specific remedy provided in official notice.
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
Spectral Instruments is recalling all Ami HT: devices because they may show a momentary absence of the X-Ray On banner during run readiness checks. This could lead to users not knowing if the device is properly set up for X-ray imaging.
The device may temporarily fail to display the X-Ray On banner during run readiness checks. This could cause users to think the device is not properly configured for X-ray imaging when it actually is, potentially leading to incorrect usage.
Users of Ami HTX devices are affected. Those who rely on the X-ray imaging function for medical or industrial purposes are most at risk.
Check for Ami HTX 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. If it does not appear, the device may be affected.
The official recall notice does not provide a remedy for this issue.
All Ami HTX devices with any serial number are affected by this recall.
The official recall notice does not specify any action steps for affected devices.
We’ve drafted a message you can send Spectral Instruments to request your refund or repair — edit it as you like.
Subject: Recall Z-2940-2026 — Spectral Instruments Spectral Instruments Hello, I own a Spectral Instruments that is covered by recall Z-2940-2026 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.
