Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 10/25/2014 510(K) Number: K123197 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative, multiplexed in vitro di... | 2 | 09/23/2014 | Nanosphere, Inc. |
Nanosphere Verigene Each CDF test consists of a Verigene CDF Nucleic Acid Test Kit and a Verigen... | 3 | 08/08/2014 | Nanosphere, Inc. |
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