Heartmate II and Heartmate 3 recall in Canada: Performance issue
In plain language
This recall involves Heartmate II and Heartmate 3 Left Ventricular Assist Systems sold in Canada. They are being recalled because a performance issue may impair the device's ability to provide adequate support. This recall is for healthcare professionals.
What to do
- Contact the manufacturer for additional information.
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Affected products
Specific affected products are listed in the official notice.
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves Heartmate II and Heartmate 3 Left Ventricular Assist Systems sold in Canada. They are being recalled because a performance issue may impair the device's ability to provide adequate support. This recall is for healthcare professionals.
What should consumers do?
Contact the manufacturer for additional 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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on March 6, 2024.
Is the THORATEC CORPORATION brand affected by this recall?
Yes, THORATEC CORPORATION products are affected by this recall. This recall involves Heartmate II and Heartmate 3 Left Ventricular Assist Systems sold in Canada. They are being recalled because a performance issue may impair the device's ability to provide adequate support. This recall is for healthcare professionals.