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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K111039
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Prox Lat Tib Lock Plate and Dist Med Tib Lock Plate Item Nos. 47235700306 47235700308 472357003... 2 11/07/2019 Zimmer Biomet, Inc.
PROX LAT HUMERAL LOCK PLATE, Item Nos. 47235800104 47235800106 47235800108 47235800112 472358001... 2 11/07/2019 Zimmer Biomet, Inc.
SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 472... 2 11/07/2019 Zimmer Biomet, Inc.
DIST LAT FEM LCK PLATE STERILE, Item Nos. 47235710106 47235710110 47235710114 47235710118 4723... 2 11/07/2019 Zimmer Biomet, Inc.
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