Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette
Brand(s)
Last updated
Summary
Product
Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette
Issue
Medical devices - Labelling and packaging
What to do
The manufacturer will contact the customers.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| Hemochron® Jr. Whole Blood Microcoaguation System - ACT-LR Test Cuvette | E5JLR132 | JACT-LR |
Issue
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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Haematology
Companies
Accriva Diagnostics, Inc.
6260 Sequence Drive, San Diego, California, United States, 92121
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-81207
Get notified
Receive emails about new and updated recall and safety alerts.