Blower/Mister recall in Canada: May cause procedural delay
In plain language
This recall involves the AXIUS Blower Mister medical device sold in Canada. It's being recalled because it may fail to emit carbon dioxide (CO2), which could lead to procedural delays during off-pump coronary artery bypass (OPCAB) surgery. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model/serial numbers if provided.
- Return, repair, or dispose of it as instructed.
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Affected products
Blower/Mister
Model: CB-1000
Lot: 96255607
Why this matters
Procedural delay
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 lot number
Lot numbers identify specific production batches.
Affected lots: 96255607
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: CB-1000
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?
Procedural delay
What should consumers do?
Stop using the product immediately. Check model/serial numbers if provided. Return, repair, or dispose of it as instructed.
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. Procedural delay
When was this product recalled?
This product was recalled on February 15, 2019.
Is the AXIUS brand affected by this recall?
Yes, AXIUS products are affected by this recall. This recall involves the AXIUS Blower Mister medical device sold in Canada. It's being recalled because it may fail to emit carbon dioxide (CO2), which could lead to procedural delays during off-pump coronary artery bypass (OPCAB) surgery. Stop using the product and follow the return/repair steps in the official notice.