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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 187 Results
Related Medical Device Recalls
 
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Product Description
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Z-2341-2017 - VITEK® 2 Gram-Negative identification card (GN), IVD, REF 21341, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2342-2017 - VITEK 2 Gram-Positive identification card (GP), IVD, REF 21342, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2343-2017 - VITEK 2 Yeast identification card (YST), IVD, REF 21343, 20 cards per carton. . 2 05/22/2017 Biomerieux Inc
Z-2344-2017 - VITEK 2 Bacillus identification card (BCL), IVD, REF 21345, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2345-2017 - VITEK 2 Neisseria-Haemophilus identification card (NH), IVD, REF 21346, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2346-2017 - VITEK 2 Anaerobic and Corynebacteria identification card (ANC), REF 21347, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2347-2017 - VITEK 2 Gram Negative Susceptibility card (AST-GN09), REF 22008, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2348-2017 - VITEK 2 Gram Negative Susceptibility card (AST-GN13), REF 22095, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2349-2017 - VITEK 2 Gram Negative Susceptibility card (AST-GN14), REF 22096, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2350-2017 - VITEK® 2 Fungal Susceptibility card (AST-YS01), REF 22108, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
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