Medical Device Recalls
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1 result found
Recall Number: Z-1793-2012 |
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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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| Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Colum... | 2 | 06/26/2015 |
FEI # 2916714 Aesculap Implant Systems |
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