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Tekia, Inc. recalls TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
Recalled November 18, 2015 · FDA recall Z-0237-2016 · Tekia
Hazard
Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power. · FDA Class II
Units
50 units
Sold at
Internationally to Vietnam.
Description
Tekia is recalling the Single Piece Hydrophillic Acrylic Intraocular Lenses (IOLs) because they may be labeled with the incorrect diopter power.
Product
TEKIA Single Piece Hydrophilic Acrylic Intraocular Lenses, Model 811
Manufacturer(s)
Tekia, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →