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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
Related Medical Device Recalls
 
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Product Description
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FDA Recall
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Z-0729-2018 - OptiView DAB IHC Detection Kit, Ventana Part Number 760-700, Roche GMMI 06396500001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0730-2018 - ultraView Universal DAB Detection Kit, Ventana part Number 760-500, Roche GMMI 05269806001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0731-2018 - iView DAB IHC Detection Kit, Ventana part Number 760-091, Roche GMMI 05266157001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0732-2018 - ultraView SISH Detection Kit, Ventana Part Number 780-001, Roche GMMI 05271967001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0733-2018 - ultraView SISH DNP Detection Kit US, Ventana Part Number 760-098, Roche GMMI 05572037001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0740-2018 - NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Ventana Part Number 760-041, Roche GMMI 05266084001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0735-2018 - CINtec PLUS Cytology Kit (Canada/Japan), Ventana Part Number 805-100, Roche GMMI 06889549001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0736-2018 - OptiView Amplification Kit, Ventana Part Number 760-099, Roche GMMI 06396518001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0737-2018 - OptiView Amplification Kit (250 Test), Ventana Part Number 860-099, Roche GMMI 06718663001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
Z-0738-2018 - Hematoxylin II, Ventana Part Number 790-22087, Roche GMMI 05277965001 in vitro diagnostic 1 02/27/2018 Ventana Medical Systems Inc
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