Medical Device Recalls
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1 result found
Recall Number: Z-1235-2016 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| KAMRA Inlay, ACI 7000 Corneal Inlay, Part No. 76195-01 and 76195-10 (OUS) Labeling: The KAMRA inl... | 2 | 03/24/2016 |
FEI # 3008401069 AcuFocus, Inc. |
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