In a flurry of Aug. 31 notices from the FDA, the number of Class I recalls plaguing Getinge’s Cardiosave intra-aortic balloon pumps this year has doubled. The notices detailed four more recalls of the ...
Getinge has recalled nearly 8,800 heart devices after receiving more than 100 complaints about them, including one report of a patient death. The recall—which began in December and came though the ...
Please provide your email address to receive an email when new articles are posted on . Datascope/Maquet/Getinge intra-aortic balloon pumps recalled due to risk for unexpected shutdown. The FDA has ...
IABP systems are typically inserted within the multidisciplinary environment that is the cardiac catheterization laboratory. The specific role of the physiologist during IABP insertion is to ensure ...
Flight nurses and paramedics at AirLift Texas bases in Waco and New Braunfels, have been trained to use the Getinge cardiosave hybrid balloon pump device during air transport, according to a July 17 ...
DUBLIN--(BUSINESS WIRE)--The "US Market Report for Intra-Aortic Balloon Pumps 2018 - MedCore" report has been added to Research and Markets' offering. An intra-aortic balloon pump system is used for ...
DUBLIN--(BUSINESS WIRE)--Research and Markets has announced the addition of the "Asia-Pacific Cardiac Assist Devices Market Outlook to 2021" report to their offering. The report provides company ...
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 ...
"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 ...