FDAFDA · Food and drugs·Recall number Z-2940-2026
Ami HTX
Published August 26, 2026 · Recall initiated: July 24, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
What to do
FDA Mandated
Recall details
- Manufacturer
- Spectral Instruments Inc
- Distributor
- United States.
- Lot
- All serial numbers.
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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