Medical Device Recalls
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1 result found
510(K) Number: K982541 |
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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 Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608 | 2 | 10/31/2019 | Becton Dickinson & Company |
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