Dvia 560 Hematology Analyzer (2016-03-11)

ADVIA 560 Hematology Analyzer Recall The ADVIA 560 Hematology Analyzer, a laboratory blood-testing device, is being recalled across Canada. The device has a Class I classification, indicating a serious issue that could result in incorrect test results. This recall affects hospitals, clinics, and other medical laboratories that use this equipment.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-04-04

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1ad7b973-d018-462c-a958-794d6401c819