AllClear
PricingSign in
FDAMay 13, 2025device

Ami HTX.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The X-ray safety and manufacturing date labels affixed to the Lago X/ AMI HTX instrument do not correspond exactly to the labeling stipulated by the FDA / CDRH.

What to do

FDA enforcement status: Ongoing

Brands named

spectral instrumentsspectral

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →