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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Recall Date to: 07/25/2014 510(K) Number: K042357
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FDA Recall
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BD Diagnostics, BD GeneOhm MRSA Assay, REF: 441242 (200 Reaction Kit) and 441244 (48 Reaction Kit). ... 2 09/10/2009 BD Diagnostics (GeneOhm Sciences, Inc)
BD GeneOhm MRSA 200 ct, Catalog #441242. IDI-MRSA assay is a qualitative in vitro diagnostic test ... 2 10/31/2008 BD Diagnostics (GeneOhm Sciences, Inc)
BD GeneOhm MRSA 48 ct, Catalog #441244. IDI-MRSA assay is a qualitative in vitro diagnostic test fo... 2 10/31/2008 BD Diagnostics (GeneOhm Sciences, Inc)
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