Medical Device Recalls
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1 result found
510(K) Number: K931368 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BD Microtainer Tube w/ BD Microgard Closure, K2EDTA additive, Model Numbers 365974 and 365975 Pro... | 2 | 07/12/2019 |
FEI # 2243072 Becton Dickinson & Company |
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