Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K160657 |
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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 Vacutainer® Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, C... | 2 | 03/26/2018 | Becton Dickinson & Company |
BD Vacutainer® Lithium Heparin Green Top Tube; Catalog Numbers: 1. 366664 (UDI: 50382903666640); 2. ... | 1 | 03/22/2018 | Becton Dickinson & Company |
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