Nidek Inc. recalls AUTO REF/KERATOMETER ARK-1s

Recalled April 18, 2018 · FDA recall Z-1348-2018 · Nidek

Hazard

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

Units

63 untis

Sold at

Distributed domestically to AK, AL, AR, CA, CO, DE, FL, GA, ID, IL, IN, MD, MI, MO, MT, NM, NY, OH, OK, PA, SC, TN, TX, VA, WA, WV.

Description

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

Product

AUTO REF/KERATOMETER ARK-1s

Manufacturer(s)

Nidek Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →