Medical Device Recalls
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1 to 3 of 3 Results
Recall Date to: 05/25/2015 510(K) Number: K042357 |
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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 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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