Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K120138 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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Kit BD Max MRSA; Catalog # 442953 | 2 | 08/22/2019 | Becton Dickinson & Co. |
The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for t... | 2 | 09/10/2014 | Becton Dickinson & Co. |
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