Medical Device Recalls
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1 result found
510(K) Number: K880636 |
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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-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro diagnostics | 3 | 04/14/2016 | Becton, Dickinson and Company, BD Biosciences |
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