Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K082078 |
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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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Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 4723580... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
DIST LAT FEM LOCK PLT, LT | 2 | 12/27/2013 | Zimmer, Inc. |
FEM COND BUTTRESS PLT, RT. | 2 | 12/27/2013 | Zimmer, Inc. |
DIST LAT FEM LOCK PLT, RT | 2 | 12/27/2013 | Zimmer, Inc. |
ITST THREADED GUIDE PIN | 2 | 12/27/2013 | Zimmer, Inc. |
FEM COND BUTTRESS PLT, LT | 2 | 12/27/2013 | Zimmer, Inc. |
ZIMMER PERIARTICULAR LOCKING PLATE SYSTEM DISTAL MEDIAL HUMERAL LOCKING PLATE, SHORT RIGHT 11 H... | 2 | 08/27/2013 | Zimmer, Inc. |
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