Laris Pump Module Model 81

Recall Summary The Alaris Pump Module Model 8100 is being recalled across Canada due to a defect classified as a serious safety issue. This device is used to deliver medications to patients. The recall affects all units of this model that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-07-06

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4ee2d442-dda6-41cb-bba7-f76cc25ddc63