Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate Recalled by Maquet Cardiovascular, LLC Due to In the Cardiosave Intra-aortic Balloon Pump, there is...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Maquet Cardiovascular, LLC directly.
Affected Products
CARDIOSAVE Intra-Aortic Balloon Pump An electromechanical system used to inflate and deflate intra-aortic balloons. It provide temporary support to the left ventricle via the principle of counterpulsation.
Quantity: 29 units (total)
Why Was This Recalled?
In the Cardiosave Intra-aortic Balloon Pump, there is a possibility that the coiled cord assembly, a prominent connector cord between the Cardiosave IABP housing and the dual display head which secured atop the IABP may fail as a result of mishandling.
Where Was This Sold?
This product was distributed to 1 state: ID
About Maquet Cardiovascular, LLC
Maquet Cardiovascular, LLC has 251 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report