Medical Device Recalls
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11 to 14 of 14 Results
Recall Date to: 08/24/2014 510(K) Number: K053536 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Zimmer Durom cup, Metasul Durom acetabular component, uncemented, 62/56, code V, Zimmer, Winterthur,... | 2 | 09/26/2008 | Zimmer Inc. |
Zimmer Durom cup, Metasul Durom acetabular component, uncemented, 64/58, code X, Zimmer, Winterthur,... | 2 | 09/26/2008 | Zimmer Inc. |
Metasul® LDH® Head Rx Sterile | 2 | 11/06/2012 | Zimmer, Inc. |
Kopf Adapter S Sterile, Rx | 2 | 11/06/2012 | Zimmer, Inc. |
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