Medical Device Recalls
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1 result found
510(K) Number: K024017 |
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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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Atellica IM HER-2/neu (H2n) assay, 50 Test Kit, Catalog No. SMN 10995591, UDI Codes: (01)0063041459... | 2 | 10/16/2020 | Siemens Healthcare Diagnostics, Inc |
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