Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K093293 |
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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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Vanguard 360 Femoral Boss Reamer, Label: REF 32-488474 VANGUARD 360 1NSTRUMENT FEMORAL BOSS REAM... | 2 | 08/15/2014 | Biomet, Inc. |
Vanguard 360 Revision Knee System Knee prostheses | 2 | 10/03/2016 | Zimmer Biomet, Inc. |
Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 ... | 2 | 09/25/2018 | Zimmer Biomet, Inc. |
Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 I... | 2 | 09/25/2018 | Zimmer Biomet, Inc. |
Vanguard 360 Revision System Posterior Augment With Bolt - Product Usage: intended for use in knee a... | 2 | 12/23/2020 | Biomet, Inc. |
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