Sena Gh And Alaris Syringe Pumps (2017-05-04)

Recall Summary Asena GH and Alaris Syringe Pumps have been recalled across Canada due to a medical device issue classified as Class I, the most serious type of recall. These pumps are used to deliver medications intravenously. The recall affects all units of these syringe pump models distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-06-05

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/511cee19-ab79-4e25-9443-b9969780e035