Home/Recalls/CANADA-57601
Health CanadaType II

iVIEW DAB, ultraView Universal DAB, ultraView SISH DNP, OptiView DAB IHC Detecti...

Published: January 12, 2018Recall ID: 57601Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

iVIEW DAB, ultraView Universal DAB, ultraView SISH DNP, OptiView DAB IHC Detection Kit and OptiView Amplification Kit, CINtec PLUS Cytology Kit, Hematoxylin II (2017-12-27)

Additional Source Details

FieldValue
N I D57601
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/iview-dab-ultraview-universal-dab-ultraview-sish-dnp-optiview-dab-ihc-detection-kit
IssueMedical devices
Title iVIEW DAB, ultraView Universal DAB, ultraView SISH DNP, OptiView DAB IHC Detection Kit and OptiView Amplification Kit, CINtec PLUS Cytology Kit, Hematoxylin II (2017-12-27)
Archived0
CategoryMedical devices
Last updated2018-01-12
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert