Ellica Im 1600 Analyzer (2018-12-12)

Atellica IM 1600 Analyzer Recall The Atellica IM 1600 Analyzer, a medical device used in laboratories, has been recalled across Canada. The device was distributed starting in 2018 and poses a serious safety risk, which is why this is classified as a Class I recall—the most serious type. This recall affects healthcare facilities and laboratories in Canada that use this analyzer.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-01-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e1aed326-3b64-430c-8cc9-508a8063707e