Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K023743 |
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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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TANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71324038, 71324039, 71324040, 71... | 2 | 11/03/2016 | Smith & Nephew, Inc. |
TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71322040, 71322041, 71322042, 7132204... | 2 | 11/03/2016 | Smith & Nephew, Inc. |
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