FDAJanuary 30, 2015device
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Power supply malfunction complaints related to suboptimal thermal management.
What to do
FDA enforcement status: Terminated
Brands named
maquet datascope corp cardiac assist divisionmaquetmaquet datascope
UPCs
099800080045099800080052099800080053099800080055
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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