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Maquet Datascope Corp - Cardiac Assist Division recalls Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
Recalled March 4, 2015 · FDA recall Z-1140-2015 · Maquet Datascope Corp - Cardiac Assist Division
Hazard
Power supply malfunction complaints related to suboptimal thermal management. · FDA Class II
Units
1,300 units
Sold at
US Nationwide distribution
Description
Power supply malfunction complaints related to suboptimal thermal management.
Product
Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
Manufacturer(s)
Maquet Datascope Corp - Cardiac Assist Division
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →