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 Recalled by Datascope Corp. Due to The power cord supplied (Type J plug end)...
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 Datascope Corp. directly.
Affected Products
MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32
Quantity: 54 units
Why Was This Recalled?
The power cord supplied (Type J plug end) for the Cardiosave Hybrid IABP to Brazil is incompatible with the Brazilian Type N power receptacle.
Where Was This Sold?
International distribution in the country of Brazil.
About Datascope Corp.
Datascope Corp. has 66 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report