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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K032396
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FDA Recall
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Modular Head Component, Biomet Hip System; Item No. 11-363661, Hip Joint, metal/polymer/metal, semi-... 2 04/27/2018 Zimmer Biomet, Inc.
36MM COCR MODULAR HD -6MM 2 03/14/2018 Zimmer Biomet, Inc.
various polyethylene implants Hips Active Articulation ArComXL Bearings Active Articulation E1 B... 2 03/27/2017 Zimmer Biomet, Inc.