Spectral Instruments Inc recalls Ami HTX
- Recalling company
- Spectral Instruments Inc
- Product
- Ami HTX
- Reason
- Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jul 24, 2026
- Reported
- Aug 26, 2026
- Distribution
- United States.
- Status
- Ongoing
- Quantity
- 35
- Lot / codes
- All serial numbers.
- Company location
- Tucson, AZ
- Recall type
- FDA Mandated
- Recall number
- Z-2940-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2940-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.