Ellica Ch 930 Analyzer (2019-08-15)

Atellica CH 930 Analyzer Recall Summary The Atellica CH 930 Analyzer, a medical laboratory device, is being recalled across Canada due to a device defect. This recall is classified as Class I, meaning there is a serious risk of adverse health consequences. The device was distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-09-12

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/397205ad-442a-43f3-a3cd-60939263685f