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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-3134-2017
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VITEK(R) 2 GP, REF 21342, IVD, UDI 03573026131920, bioMerieux, Inc. VITEK(R) 2 is an automated syst... 2 09/18/2017 FEI # 1950204
Biomerieux Inc
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