Home/Recalls/CANADA-60771
Health CanadaType III

ZYMUTEST HIA IgGAM MonoStrip (2018-02-06)

Published: March 23, 2018Recall ID: 60771Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ZYMUTEST HIA IgGAM MonoStrip (2018-02-06)

Additional Source Details

FieldValue
N I D60771
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/zymutest-hia-iggam-monostrip-2018-02-06
IssueMedical devices
Title ZYMUTEST HIA IgGAM MonoStrip (2018-02-06)
Archived0
CategoryMedical devices
Last updated2018-03-23
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert