CentriMag Extracorporeal Blood Pumping System - Motor (2019-08-22)
In plain language
This recall involves the CentriMag Extracorporeal Blood Pumping System - Motor sold in Canada. It's being recalled because electromagnetic interference can cause motor and pump issues, which may lead to serious injuries. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check the serial numbers of your CentriMag system.
- Contact Abbott for recalibration of the motor.
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Affected products
CentriMag Extracorporeal Blood Pumping System - Motor
Model: 201-10002, L201-10002
Why this matters
Serious injury due to hemodynamic compromise
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: 201-10002, L201-10002
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?
Serious injury due to hemodynamic compromise
What should consumers do?
Stop using the product immediately. Check the serial numbers of your CentriMag system. Contact Abbott for recalibration of the motor.
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. Serious injury due to hemodynamic compromise
When was this product recalled?
This product was recalled on August 30, 2019.