Laris Pk Syringe Pump

Alaris PK Syringe Pump Recall The Alaris PK Syringe Pump, a medical device used to deliver medications, is being recalled across Canada due to safety concerns. The recall is classified as Class I, meaning there is a serious risk of adverse health effects. This recall affects healthcare facilities and patients who use or may have used this syringe pump.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-10

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/af813234-3618-41fc-a98f-e07c42de95ad