Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K113550 |
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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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(1) Vanguard Knee System PS Open Box Femoral; Right; 60 mm. Intended for knee joint replacement pros... | 2 | 01/30/2023 | Biomet, Inc. |
(1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement pro... | 2 | 01/30/2023 | Biomet, Inc. |
Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126 | 2 | 11/21/2018 | Zimmer Biomet, Inc. |
Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108 | 2 | 11/21/2018 | Zimmer Biomet, Inc. |
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 ... | 2 | 06/04/2018 | Zimmer Biomet, Inc. |
Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replac... | 2 | 06/01/2018 | Zimmer Biomet, Inc. |
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
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