Medfusion Syringe Infusion Pumps recall in Canada: software defect
In plain language
This recall involves Medfusion 3500 and 4000 Syringe Infusion Pumps sold in Canada. They are being recalled because a software defect could lead to therapy delays or interruptions. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Therapy delay or interruption
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?
Therapy delay or interruption
What should consumers do?
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. Therapy delay or interruption
When was this product recalled?
This product was recalled on April 11, 2022.
Is the Smiths Medical Asd, Inc. brand affected by this recall?
Yes, Smiths Medical Asd, Inc. products are affected by this recall. This recall involves Medfusion 3500 and 4000 Syringe Infusion Pumps sold in Canada. They are being recalled because a software defect could lead to therapy delays or interruptions. Contact the manufacturer for more information.