Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 07/01/2015 510(K) Number: K082140 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Cepheid Xpert MRSA/SA Blood Culture Test for use with the GeneXpert Dx System, manufactured by Cephe... | 1 | 07/01/2010 | Cepheid |
Cepheid brand Xpert MRSA/SA-BC US-IVD, an In-vitro diagnostic test kit, Catalog Numbers: GXMRSA/SA-B... | 3 | 01/11/2012 | Cepheid |
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