Hamilton-C6 Intensive Care Ventilator recall in Canada: Performance issue
In plain language
This recall involves Hamilton-C6 Intensive Care Ventilators sold in Canada. They are being recalled because a component may have a manufacturing defect that could affect performance. Healthcare professionals should stop using the affected devices and follow the return steps in the official notice.
What to do
- Stop using the affected product immediately.
- Check the serial numbers to see if your device is affected.
- Contact your local approved distribution partner for instructions.
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Affected products
Hamilton-C6 Intensive Care Ventilator
Model: 160021
Why this matters
Performance issue
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 160021
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Performance issue
What should consumers do?
Stop using the affected product immediately. Check the serial numbers to see if your device is affected. Contact your local approved distribution partner for instructions.
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 issue
When was this product recalled?
This product was recalled on June 11, 2025.
Is the Hamilton Medical Ag brand affected by this recall?
Yes, Hamilton Medical Ag products are affected by this recall. This recall involves Hamilton-C6 Intensive Care Ventilators sold in Canada. They are being recalled because a component may have a manufacturing defect that could affect performance. Healthcare professionals should stop using the affected devices and follow the return steps in the official notice.