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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 ,

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