Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K944566 |
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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 Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes, Catalog Number 3680... | 2 | 08/21/2019 |
FEI # 2243072 Becton Dickinson & Company |
| BD Vacutainer PST Blood Collection Tubes, Catalog Number 368035, 368036 | 2 | 08/21/2019 |
FEI # 2243072 Becton Dickinson & Company |
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