Home/Recalls/CANADA-58157
Health CanadaType II

Human IgM kit for use on SPAPLUS (2018-07-25)

Published: August 2, 2018Recall ID: 58157Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Human IgM kit for use on SPAPLUS (2018-07-25)

Additional Source Details

FieldValue
N I D58157
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/human-igm-kit-use-spaplus-2018-07-25
IssueMedical devices
Title Human IgM kit for use on SPAPLUS (2018-07-25)
Archived0
CategoryMedical devices
Last updated2018-08-02
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert