Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053097 |
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Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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The VITEK 2 Gram-positive Susceptibility Card is intended for use with the VITEK 2 Systems in clinic... | 2 | 04/17/2020 | Biomerieux Inc |
bioMerieux VITEK 2 Gram Positive Cefoxitin Screen, VITEK 2 Gram Positive AST for Oxacillin, VITEK SY... | 1 | 08/30/2018 | bioMerieux, Inc. |
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