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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-0731-2018
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iView DAB IHC Detection Kit, Ventana part Number 760-091, Roche GMMI 05266157001 in vitro diagnostic 1 02/27/2018 FEI # 1000125183
Ventana Medical Systems Inc
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