Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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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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Z-3250-2018 - Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment, Model Number 185224 Intended for use in Total Knee Arthroplasty | 2 | 09/25/2018 | Zimmer Biomet, Inc. |
Z-3249-2018 - Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment, Model Number 185221 Intended for use in Total Knee Arthroplasty | 2 | 09/25/2018 | Zimmer Biomet, Inc. |
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