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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 187 Results
Related Medical Device Recalls
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Product Description
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Z-2357-2017 - VITEK 2 Gram Negative Susceptibility card (AST-N102), REF 22258, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2352-2017 - VITEK 2 Gram Positive Susceptibility card (AST-P577), REF 22218, 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-2345-2017 - VITEK 2 Neisseria-Haemophilus identification card (NH), IVD, REF 21346, 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-2350-2017 - VITEK® 2 Fungal Susceptibility card (AST-YS01), REF 22108, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2506-2017 - VITEK® 2 Fungal Susceptibility card (AST-YS08), IVD, REF 420739, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2378-2017 - VITEK® 2 Gram Fungal Susceptibility card (AST-YS05), REF 411945, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2461-2017 - VITEK® 2 Gram Fungal Susceptibility card (AST-YS07), IVD, REF 414967, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2526-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-GN04), IVD, REF 22000, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
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