Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet Datascope Corp - Cardiac Assist Division Due to Power supply malfunction complaints related to suboptimal thermal...
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 Datascope Corp - Cardiac Assist Division directly.
Affected Products
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
Quantity: 1,300 units
Why Was This Recalled?
Power supply malfunction complaints related to suboptimal thermal management.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet Datascope Corp - Cardiac Assist Division
Maquet Datascope Corp - Cardiac Assist Division has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report