Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K113848 |
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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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R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 62 MM OD, QTY: (1), STERILE H2O2, REF ... | 2 | 08/08/2013 | Smith & Nephew Inc |
R3 (TM) XLPE ACETABULAR LINER UHMWPE, 20o OVERHANG, 36 MM ID, 60 MM OD, QTY: (1), STERILE H2O2, REF ... | 2 | 08/08/2013 | Smith & Nephew Inc |
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