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U.S. Department of Health and Human Services

Medical Device Recalls
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Recall Date to: 02/28/2015 510(K) Number: K082140
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Cepheid brand Xpert MRSA/SA-BC US-IVD, an In-vitro diagnostic test kit, Catalog Numbers: GXMRSA/SA-B... 3 01/11/2012 Cepheid
Cepheid Xpert MRSA/SA Blood Culture Test for use with the GeneXpert Dx System, manufactured by Cephe... 1 07/01/2010 Cepheid
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