Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 10/23/2014 PMA Number: P060022 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Adapt AO, Akreos Advanced Optics Aspheric Lens. Bausch & Lomb Incorporated, Rochester, NY. Manufact... | 2 | 09/09/2009 | Bausch & Lomb Inc |
Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos IOL intended for primary implantation in ... | 2 | 02/20/2014 | Bausch & Lomb Surgical, Inc. |
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