Laris System (2020-06-30)

Alaris System Recall Summary The Alaris System, a medical infusion device, has been recalled across Canada due to safety concerns. The recall is classified as Class I, which indicates a serious potential health risk. This recall affects medical facilities and healthcare providers using this device across Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-07-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a3d9e74a-b90d-4864-a269-29e2f15b4280