Medical Device Recalls
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1 result found
Recall Number: Z-1037-2017 |
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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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| AFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Accessory Stent G... | 2 | 01/18/2017 |
FEI # 3011063223 Endologix |
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