Medical Device Recalls
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41 to 41 of 41 Results
Recall Date to: 08/07/2014 510(K) Number: K080991 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ASR 300 Size 64, DEPUY ASR XL ACETABULAR CUP SYSTEM. The DePuy ASR XL Acetabular Cup components a... | 2 | 03/24/2011 | Depuy Orthopaedics, Inc. |
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