Please provide your email address to receive an email when new articles are posted on . The FDA announced it has designated a recall of intra-aortic balloon pumps by Datascope/Getinge as class I, the ...
The Cardiosave Hybrid and Cardiosave Rescue intra-aortic balloon pumps (IABPs) have been hit with another recall by the manufacturer (Getinge/Datascope), this time due to damage to the balloon ...
"In short, it seems likely that the returned arterialized blood should be returned during diastole when the aortic valve is closed. This would probably offer less resistance to the ailing heart's ...
Among the top stories in cardiology this week was an FDA recall of intra-aortic balloon pumps and a report that explained how icosapent ethyl improved outcomes in adults with elevated CV risk that are ...
Maquet/Datascope intra-aortic balloon pumps (IABPs) may be at risk of shutting down while running on batteries, failure of their batteries to charge, or premature battery depletion, the US Food and ...
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