Medical Device Recalls
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1 result found
510(K) Number: K983952 |
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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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VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Hold... | 2 | 01/17/2020 | Greiner Bio-One North America, Inc. |
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