Bd Alaris™ Pump Module And Subset Of Compatible Pump Infusion Sets

Recall Summary BD is recalling certain Alaris Pump Modules and compatible pump infusion sets distributed in Canada due to a performance issue. The recall affects specific batches of these infusion pump products used for delivering medications. This is classified as a Class I recall, indicating a serious potential health impact.

Product

BD Alaris™ Pump Module and subset of Compatible Pump Infusion Sets

Reason

Device performance issue

Classification

Class II

Category

medical device recall

Country

Canada

Agency

HC-DEVICES

Recall date

2026-09-28

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/47f4615f-e7b9-4713-9c35-54e15a4a2af6