FDA · Medical devices ·
Ami HTX recall
Spectral Instruments Inc recalled Ami HTX on August 26, 2026 because of momentary absence of On-Screen "X-Ray On" banner during run readiness check. It was sold in United States..
Why it was recalled
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
What's recalled
Ami HTX
Quantity: 35
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Spectral Instruments Inc, Tucson, AZ
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- United States.
- Status
- Ongoing
- Recall number
- Z-2940-2026
- Source
- U.S. Food and Drug Administration
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