Ami HTX recall
Ami HTX
Why was Ami HTX recalled?
Momentary absence of On-Screen "X-Ray On" banner during run readiness check.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
All serial numbers.
- Product
- Ami HTX
- Recalling firm
- Spectral Instruments Inc
- Quantity
- 35
- Distribution
- United States.
- Recall date
- August 26, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)