Getinge subsidiary Datascope has another aortic pump recall

The Cardiosave Hybrid system. [Image from FDA]The FDA issued a notice labeling another recall of Getinge subsidiary Datascope’s Cardiosave pump as Class I, the most serious kind.
This recall relates to the Swedish medtech company’s Cardiosave Hybrid and Cardiosave Rescue intra-aortic…

Source: www.massdevice.com – Read more