Home/Recalls/CANADA-58479
Health CanadaType II

Human IgM kit for use on SPAPLUS (2018-10-23)

Published: November 15, 2018Recall ID: 58479Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Human IgM kit for use on SPAPLUS (2018-10-23)

Additional Source Details

FieldValue
N I D58479
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/human-igm-kit-use-spaplus-2018-10-23
IssueMedical devices
Title Human IgM kit for use on SPAPLUS (2018-10-23)
Archived0
CategoryMedical devices
Last updated2018-11-15
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert