Home/Recalls/CANADA-81207
Health CanadaType II

Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette

Published: November 13, 2025Recall ID: 81207Category: generalCountry: Canada

Reason for Recall / Hazard

Labelling and packaging

Product Description & Identification

Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette

Additional Source Details

FieldValue
N I D81207
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/hemochronr-jr-whole-blood-microcoaguation-system-act-lr-test-cuvette
IssueLabelling and packaging
TitleHemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette
ProductHemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette
Archived0
CategoryHaematology
Last updated2025-11-13
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert