Alcon Research, Ltd. recalls Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following c

Recalled January 18, 2017 · FDA recall Z-0978-2017 · Alcon Research

Hazard

The intraocular lens could become lodged within the cartridge · FDA Class II

Units

1,130 units

Sold at

Distributed to Mexico only

Description

The intraocular lens could become lodged within the cartridge

Product

Alcon Monarch III (1) "C" Cartridge The device is used for implanting AcrySof intraocular lenses in the eye following cataract removal

Manufacturer(s)

Alcon Research, Ltd.

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