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Bausch & Lomb Surgical, Inc. recalls Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of
Recalled February 26, 2014 · FDA recall Z-1062-2014 · Bausch & Lomb Surgical
Hazard
Lens was manufactured with incorrect raw material. · FDA Class II
Units
336 IOLs (283 IOLs in the US, 53 IOLs outside the US)
Sold at
Worldwide Distribution: US (nationwide) and Internationally to: Great Britain, France, Spain, Portugal, Sweden, Russia and Guadeloupe.
Description
Lens was manufactured with incorrect raw material.
Product
Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in the capsular bag of the eye for the visual correction of aphakia secondary to the removal of a cataractous lens in adult patients.
Manufacturer(s)
Bausch & Lomb Surgical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →