Medical Device Recalls
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1 result found
510(K) Number: K071143 |
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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 Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FIT... | 3 | 08/09/2016 | Becton, Dickinson and Company, BD Biosciences |
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