ProductGuru Recalls

Official recall record

CentriMag™ Adult ECMO Kit and Blood Pump

Health Canada — Medical Devices · 2025-10-22 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-10-22
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Abbott is initiating a voluntary recall customer notification to remind customers that when using the CentriMag™ Acute Circulatory Support System you must always ensure the CentriMag™ blood pump is securely locked into the CentriMag™ motor as described in the instructions for use (IFU). Failure to properly lock the blood pump into the motor could lead to particulate or increased heat while using the system. At this time, Abbott is not requesting that this product be returned or removed from the field. If the pump is able to be locked into the motor, the product is safe for use and functions as intended when the IFU is followed to securely seat the pump.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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