BEUDAMED
    44 results · 13ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Recall × Status: Terminated × Clear all

    iVIEW DAB Detecion Kit. Catalog Number 760-091

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code KTO·May 7, 2003

    iView DAB IHC Detection Kit, Ventana part Number 760-091, Roche GMMI 05266157001 in vitro diagnostic

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·December 19, 2017

    ultraView Universal DAB Detection Kit, Ventana part Number 760-500, Roche GMMI 05269806001 in vitro diagnostic

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·December 19, 2017

    OptiView DAB IHC Detection Kit, Ventana Part Number 760-700, Roche GMMI 06396500001 in vitro diagnostic

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·December 19, 2017

    iView DAB Detection Kit, Catalog Number 05266157001, model 760-091 Immunohistochemistry (IHC) for in vitro diagnostic use.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·August 2, 2018

    iView DAB Detection Kit w/o Secondary Antibody, Catalog Number 05266173001, Model 760-093. For laboratory use.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·August 2, 2018

    OptiView DAB IHC Detection Kit, Catalog Number 06396500001, model 760-700 Immunohistochemistry (IHC) for in vitro diagnostic use.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·August 2, 2018

    ultraView Universal DAB Detection Kit, Catalog Number 05269806001, model 760-500 Immunohistochemistry (IHC) for in vitro diagnostic use.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·August 2, 2018

    NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Ventana Part Number 760-041, Roche GMMI 05266084001 in vitro diagnostic

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·December 19, 2017

    NEXES VEN IVIEW DAB DET KT JPN-US EXPORT, Catalog Number 05266084001 Model 760-041 Immunohistochemistry (IHC) for in vitro diagnostic use.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code NJT·August 2, 2018

    Intralase FS Laser System. Laser Keratome

    FDA Recall
    Terminated ·Product code GEX·July 15, 2003

    Welch Allyn AED 10 automated external defibrillator and MRL Jumpstart (collectively "AED 10")

    FDA Recall
    Terminated ·Welch Allyn Protocol, Inc·Product code MKJ·February 26, 2009

    iView DAB Detection Kit, Part number: 760-091 (05266157001) This detection kit is intended for in vitro diagnostic use. Ventana Medical Systems' (Ventana) iVIEW DAB Detection Kit is an indirect biotin streptavidin system for detecting mouse IgG, mouse IgM and rabbit primary antibodies. The kit is intended for laboratory use to identify targets by immunohistochemistry (IHC) in sections of formalin fixed, paraffin embedded and frozen tissue on Ventana Medical Systems (Ventana) automated slide stainers by light microscopy. The clinical interpretation of any staining, or the absence of staining, must be complemented by morphological studies and evaluation of proper controls. Evaluation must be made by a qualified pathologist within the context of the patient's clinical history and other diagnostic tests.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code MYA·May 16, 2011

    ultraView Universal DAB Detection Kit, Part number: 760-500 (05269806001) This detection kit is intended for in vitro diagnostic use. Ventana Medical Systems' (Ventana) iVIEW DAB Detection Kit is an indirect biotin streptavidin system for detecting mouse IgG, mouse IgM and rabbit primary antibodies. The kit is intended for laboratory use to identify targets by immunohistochemistry (IHC) in sections of formalin fixed, paraffin embedded and frozen tissue on Ventana Medical Systems (Ventana) automated slide stainers by light microscopy. The clinical interpretation of any staining, or the absence of staining, must be complemented by morphological studies and evaluation of proper controls. Evaluation must be made by a qualified pathologist within the context of the patient's clinical history and other diagnostic tests.

    FDA Recall
    Terminated ·Ventana Medical Systems Inc·Product code MYA·May 16, 2011

    Oasis Dry Suction Water Seal Chest Drain, DRY SINGLE W/AC P/N: 3600-100

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code PAD·May 7, 2015

    Ocean Water Seal Chest Drain, Single Collection W/AC, P/N: 2002-000

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code PAD·May 7, 2015

    EXPRESS Dry Seal Chest Drain, Single Collection P/N: 4000-100N

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code PAD·May 7, 2015

    Ocean Water Seal Chest Drain, SINGLE W/AC P/N: 2002-100

    FDA Recall
    Terminated ·Atrium Medical Corporation·Product code PAD·May 7, 2015

    Eridan Automated Slide Stainer and Support Cart, REF E300 and E300SC1, Dako Colorado, Inc. (Catalog No. (ER 00130,00331,00230,00431)

    FDA Recall
    Terminated ·Dako Colorado, Inc.·Product code KPA·October 2, 2006

    PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.

    FDA Recall
    Terminated ·Dako North America Inc.·Product code IDY·May 1, 2008