Hemochron® Jr. Whole Blood Microcoaguation System - Act-lr Test Cuvette

Recall Summary The Hemochron® Jr. Whole Blood Microcoagulation System ACT-LR Test Cuvette is being recalled across Canada due to labelling and packaging issues. This is a Class I recall, which means the product could cause serious health problems or death. The affected product is a medical device used for blood coagulation testing.

Product

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

Reason

Labelling and packaging

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2025-11-13

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ec0e72a0-c031-424f-bd2f-d1cc92e651a1