Medical Device Recalls
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11 to 11 of 11 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0139-2016 - ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US) M5722INT0600210 (OUS) | 2 | 10/21/2015 |
FEI # 3009844603 ConforMIS, Inc. |
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