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U.S. Department of Health and Human Services

Medical Device Recalls
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Z-2295-2010 - VITEK TWO AST-N085 REF 22 225 For In Vitro Diagnostic Use - each test card is packaged into a foil pouch with 20 pouches per box. The firm name on the label is bioMerieux, Inc., Durham, NC and bioMer... 2 08/27/2010 Biomerieux Inc
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