Centry System Hemodialysis Blood Tubing Set recall in Canada: kinked lines
In plain language
This recall involves the Centry System Hemodialysis Blood Tubing Set and Cartridge sold in Canada. It's 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 model numbers.
- Return the product as instructed.
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Affected products
CENTRY SYSTEM HEMODIALYSIS BLOOD TUBING SET
Model: 101025, 101290, 103402, 106289, 114434
Lot: All lots
HOSPAL CARTRIDGE WITH HEMOSCAN
Model: 114510
Lot: All lots
CARTRIDGE LOW WEIGHT LOW VOLUME
Model: 114613
Lot: All lots
Why this matters
Kinked access lines
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: 101025, 101290, 103402, 106289, 114434, 114510, 114613
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 access lines
What should consumers do?
Stop using the product immediately. Check model numbers. Return the product 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. Kinked access lines
When was this product recalled?
This product was recalled on January 15, 2021.
Is the Centry System brand affected by this recall?
Yes, Centry System products are affected by this recall. This recall involves the Centry System Hemodialysis Blood Tubing Set and Cartridge sold in Canada. It's being recalled because the access lines may kink during treatment. Stop using the product and follow the return steps in the official notice.