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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1062-2014
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Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in ... 2 02/20/2014 FEI # 1119279
Bausch & Lomb Surgical, Inc.
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