Medical Device Recalls
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1 result found
510(K) Number: K980858 |
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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 FACSCalibur; Catalog Numbers 342973, 342975, 34976 In vitro Diagnostics Use. | 2 | 06/26/2015 | BD Biosciences, Systems & Reagents |
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