FDAFebruary 1, 2017device

Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System. Ophthalmic laser system use for correction of corneal refraction and ablation of the corneal surface. The system is composed of a laser generator which produces an excimer laser radia...

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

The hazard

During treatment planning, the procedure was programmed with an unintended (wrong) correction.

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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