Home/Recalls/CANADA-82075
Health CanadaType II

directCHECK™ Whole Blood Control

Published: May 14, 2026Recall ID: 82075Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

directCHECK™ Whole Blood Control

Affected Products

directCHECK™ Whole Blood Control

Additional Source Details

FieldValue
N I D82075
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/directchecktm-whole-blood-control
IssueLabelling and packaging
TitledirectCHECK™ Whole Blood Control
ProductdirectCHECK™ Whole Blood Control
Archived0
CategoryHaematology
Last updated2026-05-14
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert