Sequestra 1000 System recall in Canada: risk of blood loss
In plain language
This recall involves the Sequestra 1000 System, a medical device used in Canada. It's being recalled because Y-connectors in the suction lines may tear or crack, which could lead to leaks. Leaks could cause blood loss and a breach in the system's circuit. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check the model numbers: BT920, BT926, BTC93.
- Contact Medtronic Inc. for more information.
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Affected products
Sequestra 1000 System
Model: BT920, BT926, BTC93
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Risk of blood loss
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: BT920, BT926, BTC93
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?
Risk of blood loss
What should consumers do?
Stop using the product immediately. Check the model numbers: BT920, BT926, BTC93. Contact Medtronic Inc. 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. Risk of blood loss
When was this product recalled?
This product was recalled on January 8, 2019.