Datascope Corp./MAQUET Recalls Intra-Aortic Balloon Pumps Due to False Blood Detection Alarm and Ingress of Fluid into the Intra-Aortic Balloon Pump

The FDA has identified this as a Class I recall, the most serious type of recall.  Use of these devices may cause serious injuries or death. Recalled Product(s): Datascope Corp./MAQUET Intra-Aortic Balloon Pump Model/Item Numbers: CS100i, CSO100, CS300 Lot Numbers: All Lots
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