Bd Alaris™ Infusion Devices

BD Alaris™ Infusion Devices Recall Summary BD Alaris™ Infusion Devices are being recalled across Canada due to a device compatibility issue. This is a Class I recall, which indicates a serious problem. The recall affects infusion devices distributed throughout Canada.

Product
BD Alaris™ Infusion Devices
Reason
Device compatibility
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-10-30
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/be5270e7-3eae-40c4-a4bb-1a6300d59b9c