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U.S. Department of Health and Human Services

Medical Device Recalls

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111 to 114 of 114 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0282-2011 - VITEK 2 Gram Negative Susceptibility Card, AST-GN40, REF 410 756, For In Vitro Diagnostic Use, 20 cards/box. The firm names on the label are bioMerieux, Inc., Durham, NC, and bioMerieux sa, 69280 Ma... 1 11/11/2010 Biomerieux Inc
Z-0283-2011 - VITEK 2 Gram Negative Susceptibility Card, AST-GN43, REF 410 759, For In Vitro Diagnostic Use, 20 cards/box. The firm names on the label are bioMerieux, Inc., Durham, NC, and bioMerieux sa, 69280 Ma... 1 11/11/2010 Biomerieux Inc
Z-0284-2011 - VITEK 2 Gram Negative Susceptibility Card, AST-GN44, REF 410 805, For In Vitro Diagnostic Use, 20 cards/box. The firm names on the label are bioMerieux, Inc., Durham, NC, and bioMerieux sa, 69280 Ma... 1 11/11/2010 Biomerieux Inc
Z-0285-2011 - VITEK 2 Gram Negative Susceptibility Card, AST-N107, REF 22 265, For In Vitro Diagnostic Use, 20 cards/box. The firm names on the label are bioMerieux, Inc., Durham, NC, and bioMerieux sa, 69280 Mar... 1 11/11/2010 Biomerieux Inc
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