Utomated Digital Cell Morphology Analyzer Di-6

Recall Summary The Automated Digital Cell Morphology Analyzer DI-60 device is being recalled in Canada because it may not accurately classify blood cells, which could lead to incorrect test results. The recall affects healthcare facilities and laboratories across Canada that use this blood analysis equipment.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-09-16

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3fb4243f-6500-4126-add3-7a37b2edf7d0