Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K142933 |
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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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MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM ... | 3 | 06/11/2015 | Biomet, Inc. |
Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 14... | 2 | 06/01/2018 | Zimmer Biomet, Inc. |
Vanguard Total Knee, PUNCH THRU TRL PLATES, 63 MM Item No: 32-487261, 67 MM Item No: 32-487262, 71 M... | 2 | 02/16/2017 | Zimmer Biomet, Inc. |
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