FDADecember 20, 2017device

AUTO REF/KERATOMETER ARK-1s

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

The hazard

There is possibly a difference between the measured dioptric value of the subjective measurement mode and the objective measurement mode on ARK-1s.

What to do

FDA enforcement status: Terminated

Brands named

nidek

Recall history

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

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AUTO REF/KERATOMETER ARK-1s — Recall Details · AllClear