Getinge's cardiac device sees 5th recall notice in 2023

About 16,000 Getinge Cardiosave Hybrid and Rescue Intra-aortic Balloon Pumps have been recalled due to risks of the balloon breaking, power failures and circuit board communication failures.

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, Cardiosave Hybrid , Rescue Intra Aortic Balloon Pumps , Intra Aortic Balloon Pumps , Fda , Medical Device Recall , Ardiology , Balloon , Injuries , Deaths , Oiled Cord Connection , Ircuit Board Communication , Udden Power Failure ,