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Alcon LenSx, Inc. recalls Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulot
Recalled April 16, 2014 · FDA recall Z-1445-2014 · Alcon LenSx
Hazard
Alcon LenSx received reports of unexpected downward motion of the gantry. · FDA Class II
Units
75
Sold at
Worldwide Distribution.
Description
Alcon LenSx received reports of unexpected downward motion of the gantry.
Product
Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofragmentation.
Manufacturer(s)
Alcon LenSx, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →