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U.S. Department of Health and Human Services

Medical Device Recalls

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161 to 170 of 187 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-2501-2017 - VITEK¿ 2 Gram Negative Susceptibility card (AST-N340), IVD, REF 419412, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2502-2017 - VITEK¿ 2 Gram Positive Susceptibility card (AST-P645), IVD, REF 419602, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2503-2017 - VITEK¿ 2 Gram Positive Susceptibility card (AST-P646), IVD, REF 420144, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2504-2017 - VITEK¿ 2 Gram Negative Susceptibility card (AST-N344), IVD, REF 420440, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2505-2017 - VITEK¿ 2 Gram Negative Susceptibility card (AST-N345), IVD, REF 420580, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2506-2017 - VITEK¿ 2 Fungal Susceptibility card (AST-YS08), IVD, REF 420739, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2507-2017 - VITEK¿ 2 Gram Negative Susceptibility card (AST-N348), IVD, REF 420856, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2508-2017 - VITEK¿ 2 Gram Positive Susceptibility card (AST-P648), IVD, REF 420857, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2509-2017 - VITEK¿ 2 Gram Positive Susceptibility card (AST-P649), IVD, REF 420858, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
Z-2510-2017 - VITEK¿ 2 Streptococcus Susceptibility card (AST-ST02), IVD, REF 420915, 20 cards per carton. 2 05/22/2017 FEI # 1950204
Biomerieux Inc
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