Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K033612 |
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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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Factor II (prothrombin) G20210A kit, catalog number 03610195001, Roche Diagnostics, Indianapolis,... | 2 | 03/14/2011 | Roche Diagnostics Operations, Inc. |
FACTOR II (PROTHROMBIN) G20210A Kit, LightCycler 2.0 Instrument. Material Number 03610195 001 Cont... | 2 | 03/05/2010 | Roche Molecular Systems, Inc. |
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