Health products• Updated Mar 31• Carefusion 303, Inc.
Alaris & BD Alaris Point-Of-Care Unit (PCU)
This recall involves Alaris and BD Alaris Point-Of-Care Units (PCU) sold in Canada. It's being recalled because incorrec...
Carefusion 303, Inc. Recalls in Canada
All product recalls associated with Carefusion 303, Inc. in Canada, sourced from Health Canada, Transport Canada, and the CFIA.
7 recalls
Most recent: Feb 20, 2026
Medical devices• Updated Jan 3• Carefusion 303, Inc.
BD Alaris™ Pump Module recall in Canada: Performance issues
This recall involves the BD Alaris™ Pump Module sold in Canada. It's being recalled because dropping the device may caus...
Medical devices• Updated Jan 3• Carefusion 303, Inc.
BD Alaris™ Pump Module recall in Canada: performance issues
This recall involves the BD Alaris™ Pump Module and a subset of compatible pump infusion sets sold in Canada. They are b...
Medical devices• Updated Jan 3• Carefusion 303, Inc.
Alaris™ Pump Module recall in Canada: Device compatibility issue
This recall involves Alaris™ Pump Module and BD Alaris™ Pump Module in Canada. It's being recalled because of a device c...
Medical devices• Updated Jan 3• Carefusion 303, Inc.
BD Alaris PCU recall in Canada: performance issue
This recall involves the BD Alaris PCU, a medical device used in healthcare settings. It's being recalled because bent c...
Medical devices• Updated Jan 3• Carefusion 303, Inc.
BD Alaris Infusion Devices recall in Canada: Device compatibility issue
This recall involves BD Alaris Infusion Devices sold in Canada. It's being recalled because certain syringes have not be...
Medical devices• Updated Jan 3• Carefusion 303, Inc.
BD Alaris Large Volume Pump recall in Canada: Over or under infusion risk
This recall involves the BD Alaris Large Volume Pump sold in Canada. It's being recalled because a loose or incorrect sc...