Home/Recalls/CANADA-61973
Health CanadaType II

API PHARMA COVID-RAPID ANTIGEN TEST (2020-12-18)

Published: December 31, 2020Recall ID: 61973Category: generalCountry: Canada

Reason for Recall / Hazard

COVID - Medical devices

Product Description & Identification

API PHARMA COVID-RAPID ANTIGEN TEST (2020-12-18)

Additional Source Details

FieldValue
N I D61973
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/api-pharma-covid-rapid-antigen-test-2020-12-18
IssueCOVID - Medical devices
Title API PHARMA COVID-RAPID ANTIGEN TEST (2020-12-18)
Archived0
CategoryMedical devices
Last updated2020-12-31
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert