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Hemochron® jr. Whole blood microcoaguation system - act-lr test cuvette
Official notice
13 Nov 2025
Last checked
13 Nov 2025
An official Health Canada notice concerns Hemochron® jr. Whole blood microcoaguation system - act-lr test cuvette. A complaint was received from a customer about finding a foreign object (single edge blade) inside one (1) Hemochron® JACT-LR test cartridge. There have been no adverse events reported to date. Published 2025-11-13.
What to do now
The manufacturer will contact the customers.
Recall number
81207
Official notice
2025-11-13
The hazard
The hazard
A complaint was received from a customer about finding a foreign object (single edge blade) inside one (1) Hemochron® JACT-LR test cartridge. There have been no adverse events reported to date.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Turn on recall alertsAffected products
Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Manufacturer
Phone
Brand: Accriva Diagnostics, Hemochron® Jr Whole Blood Microcoaguation System - Act-lr Test Cuvette.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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