BD Alaris™ Pump Module recall in Canada: performance issues
In plain language
This recall involves the BD Alaris™ Pump Module and a subset of compatible pump infusion sets sold in Canada. They are being recalled because of performance issues, particularly at low infusion rates. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer if you require additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Specific affected products are listed in the official notice.
Why this matters
Performance issues
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Performance issues
What should consumers do?
Stop using the product immediately. Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Performance issues
When was this product recalled?
This product was recalled on September 24, 2025.
Is the Carefusion 303, Inc. brand affected by this recall?
Yes, Carefusion 303, Inc. products are affected by this recall. This recall involves the BD Alaris™ Pump Module and a subset of compatible pump infusion sets sold in Canada. They are being recalled because of performance issues, particularly at low infusion rates. Stop using the product and contact the manufacturer for more information.