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U.S. Department of Health and Human Services

Medical Device Recalls

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41 to 50 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-2381-2017 - VITEK® 2 Gram Positive Susceptibility card (AST-P621), REF 412533, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2382-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N190), REF 412548, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2383-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N193), REF 412604, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2384-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N194), REF 412605, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2385-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-GN65), REF 412608, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2386-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N195), REF412609, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2387-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N201), REF 412862, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2388-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N202), REF 412863, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2389-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N203), REF 412864, 20 cards per carton. 2 05/22/2017 Biomerieux Inc
Z-2390-2017 - VITEK® 2 Gram Negative Susceptibility card (AST-N204), REF 412865, 20 cards per carton. . 2 05/22/2017 Biomerieux Inc
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