Artiset Blood Tubing Set recall in Canada: Kinked lines
In plain language
This recall involves Artiset Blood Tubing Sets used for hemodialysis in Canada. They are being recalled because the access lines may kink during treatment. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model numbers provided.
- Contact Baxter Corporation for more information.
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Affected products
ARTISET BLOOD TUBING SET FOR HAEMODIALYSIS HD SN HC
Model: 114533
Lot: All lots
ARTISET BLOOD TUBING SET FOR HAEMODIALYSIS- HD DNL HC
Model: 955075
Lot: All lots
Why this matters
Kinked lines during treatment
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 114533, 955075
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?
Kinked lines during treatment
What should consumers do?
Stop using the product immediately. Check the model numbers provided. Contact Baxter Corporation for more 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. Kinked lines during treatment
When was this product recalled?
This product was recalled on January 15, 2021.
Is the Artiset brand affected by this recall?
Yes, Artiset products are affected by this recall. This recall involves Artiset Blood Tubing Sets used for hemodialysis in Canada. They are being recalled because the access lines may kink during treatment. Stop using the product and follow the return steps in the official notice.