Product Wiki · Recalls · U.S. FDA — Device Enforcement

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. — recall Z-1062-2014

U.S. FDA — Device Enforcement · United States · 2013-10-16 · Class II

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1062-2014
Date of alert
2013-10-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Bausch & Lomb Surgical, Inc.
Product category
device
Product type
Devices
Reported risk: Lens was manufactured with incorrect raw material.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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