Medical Device Recalls
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1 result found
510(K) Number: K012787 |
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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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REFLECTION(R), MICROSTABLE(R), ACETABULAR LINER, 20o OVERHANG, 28 MM ID, 54-56 OD, QTY: (1), STERILE... | 2 | 12/26/2013 | Smith & Nephew Inc |
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