Home/Recalls/CANADA-63807
Health CanadaType II

Simplexa Covid-19 Direct Assay

Published: January 10, 2022Recall ID: 63807Category: generalCountry: Canada

Reason for Recall / Hazard

Manufacturing defect

Product Description & Identification

Simplexa Covid-19 Direct Assay

Additional Source Details

FieldValue
N I D63807
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/simplexa-covid-19-direct-assay
IssueManufacturing defect
TitleSimplexa Covid-19 Direct Assay
ProductSimplexa Covid-19 Direct Assay
Archived0
CategoryMedical devices
Last updated2022-01-10
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert