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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K113550
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Product Description
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FDA Recall
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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 FEI # 1825034
Biomet, Inc.
(1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement pro... 2 01/30/2023 FEI # 1825034
Biomet, Inc.
Vanguard Complete Knee System; E1 Vanguard PS Tibial Bearing; Model Numbers EP-183664, EP-183642 ... 2 06/04/2018 FEI # 1825034
Zimmer Biomet, Inc.
Vanguard Knee System PS Tibial Bearing, Part Number 183621 Intended for use in knee joint replac... 2 06/01/2018 FEI # 1825034
Zimmer Biomet, Inc.
Vanguard CR Porous Femoral 62.5mm (Left Femur) For use in total knee arthroplasty 2 03/14/2018 FEI # 1825034
Zimmer Biomet, Inc.
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