Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K081920 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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 #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. |
BD GeneOhm Cdiff Assay, Catalog 441401, 200 tests/kit, labeled, in part ***BD Diagnostics, 2555 Boul... | 3 | 08/05/2010 | Becton Dickinson & Co. |
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