CanadaHemochron Jr. Whole Blood Microcoagulation System — ACT‑LR Test Cuvette (Lot E5JLR132; model/catalogue JACT‑LR) is affected. A customer complaint reported a foreign object (single edge blade) inside one JACT‑LR test cartridge; no adverse events have been reported. The manufacturer will contact customers.
What's being recalled
Companies: Accriva Diagnostics, Inc., 6260 Sequence Drive, San Diego, California, United States, 92121.
How to identify it
Affected products: Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette; Lot or serial number: E5JLR132; Model or catalogue number: JACT-LR
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.
What to do
The manufacturer will contact the customers.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)
United States