Home/Recalls/CANADA-58026
Health CanadaType III

ZYMUTEST HIA IGGAM (2017-11-09)

Published: November 30, 2017Recall ID: 58026Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

ZYMUTEST HIA IGGAM (2017-11-09)

Additional Source Details

FieldValue
N I D58026
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/zymutest-hia-iggam-2017-11-09
IssueMedical devices
Title ZYMUTEST HIA IGGAM (2017-11-09)
Archived1
CategoryMedical devices
Last updated2017-11-30
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert