Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 09/16/2014 510(K) Number: K093346 |
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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 MRSA ACP Assay, Catalog #441639, box 200 tests labeled in part***GeneOhm Sciences Canada,... | 2 | 09/06/2012 | Becton Dickinson & Co. |
BD GeneOhm MRSA ACP Assay Catalog #441637, box 48 tests labeled in part***GeneOhm Sciences Canada, I... | 2 | 09/06/2012 | Becton Dickinson & Co. |
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