Home/Recalls/CANADA-59770
Health CanadaType III

Optilite IgM Kit (2019-07-19)

Published: August 16, 2019Recall ID: 59770Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

Optilite IgM Kit (2019-07-19)

Additional Source Details

FieldValue
N I D59770
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/optilite-igm-kit-2019-07-19
IssueMedical devices
Title Optilite IgM Kit (2019-07-19)
Archived0
CategoryMedical devices
Last updated2019-08-16
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert