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Alcon Research LLC recalls Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY SYST
Recalled June 17, 2020 · FDA recall Z-2287-2020 · Alcon Research
Hazard
Incorrect IOL diopter · FDA Class II
Units
84 units
Sold at
US Nationwide distribution including in the states of TX, PA, CT, IA, MI, NE.
Description
Incorrect IOL diopter
Product
Acrysof, IQ IOL w/UltraSert System, AcrySof IQ ASPHERIC IOL, 20.5 D, SP ACRYLIC FOLDABLE LENS, w/UltraSert DELIVERY SYSTEM, UV w/BLUE LIGHT FILTER. 13.0mm. LENGTH, 6.0mm ANTERIOR ASYMMETRIC BICONVEX OPTIC, PLANAR HAPTICS.
Manufacturer(s)
Alcon Research LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →