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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 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-2361-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-GP69), REF 22304, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2362-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P600), REF 22313, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2363-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P603), REF 22320, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2364-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P605), REF 22325 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2365-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P606), REF 22330, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2366-2017 - VITEK 2 Gram Negative Susceptibility card (AST-GN38), REF 22331, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2367-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P607), REF 22335, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2368-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P608), REF 22336, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2369-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P612), REF 22359, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2370-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-XN01), REF 410025, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
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