Home/Recalls/CANADA-59882
Health CanadaType III

ZYMUTEST HIA MonoStrip IgG & IgGAM(2019-07-23)

Published: August 9, 2019Recall ID: 59882Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ZYMUTEST HIA MonoStrip IgG & IgGAM(2019-07-23)

Additional Source Details

FieldValue
N I D59882
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/zymutest-hia-monostrip-igg-iggam2019-07-23
IssueMedical devices
Title ZYMUTEST HIA MonoStrip IgG & IgGAM(2019-07-23)
Archived0
CategoryMedical devices
Last updated2019-08-09
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert