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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Recall Date to: 04/19/2015 510(K) Number: K081920
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BD GeneOhm Cdiff Assay, Part #441401, containing Lysis Kit sample buffer tubes, 200 tests/kit; label... 2 01/17/2014 Becton Dickinson & Co.
BD GeneOhm Cdiff Assay, Catalog 441401, 200 tests/kit, labeled, in part ***BD Diagnostics, 2555 Boul... 3 08/05/2010 Becton Dickinson & Co.
BD GeneOhm Cdiff Assay , Catalog #441400 200, box tests 1-3 labeled in part***BD Diagnostics, 2555 b... 2 09/06/2012 Becton Dickinson & Co.
BD GeneOhm Cdiff Assay , Catalog # 441401, 200 box tests 2-3 labeled in part***GeneOhm Sciences C... 2 09/06/2012 Becton Dickinson & Co.
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