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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0093-06 - Tecnis Monofocal Silicone Posterior Chamber IOLs (Models: Z9000 and Z9001) 2 10/28/2005 Advanced Medical Optics, Inc.
Z-0094-06 - Tecnis Multifocal Silicone Posterior Chamber IOLs (Model: ZM900) 2 10/28/2005 Advanced Medical Optics, Inc.
Z-0097-06 - CeeOn Heparin SurfaceModifie (HSM) PMMA One-Piece Anterior Chamber IOLs (Model: HSM65) 2 10/28/2005 Advanced Medical Optics, Inc.
Z-0096-06 - CeeOn Heparin Surface Modified (HSM) PMMA One-Piebe Posterior Chambet- IOLs (Models:722C, 722Y, 811C, 812C and 812CU) 2 10/28/2005 Advanced Medical Optics, Inc.
Z-0095-06 - CeeOn EDGE Silicone Posterior Chamber IOLs (Modelsl 911A and 913A) 2 10/28/2005 Advanced Medical Optics, Inc.
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