Medical Device Recalls
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11 to 14 of 14 Results
Recall Date to: 05/24/2015 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, 66/60, code Z, Zimmer, Winterthur,... | 2 | 09/26/2008 | Zimmer Inc. |
Zimmer Durom cup, Metasul Durom acetabular component, uncemented, 46/40, code F, Zimmer, Winterthur,... | 2 | 09/26/2008 | Zimmer Inc. |
Zimmer Durom cup, Metasul Durom acetabular component, uncemented, 44/38, code D, Zimmer, Winterthur,... | 2 | 09/26/2008 | Zimmer Inc. |
Zimmer Durom cup, Metasul Durom acetabular component, uncemented, 56/50, code P, Zimmer, Winterthur,... | 2 | 09/26/2008 | Zimmer Inc. |
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