— Datascope Corp./Maquet initiated a voluntary worldwide field correction of some of its intra-aortic balloon pumps (IABPs) due to a potential mechanical failure of the fan assembly associated with ...

The US Food and Drug Administration (FDA) continues to receive reports of device failures associated with Maquet/Datascope Cardiosave Hybrid, Cardiosave Rescue, CS300, and CS100/CS100i intra-aortic ...

Pune, Maharashtra, India, August 31 2020 (Wiredrelease) Prudour Pvt. Ltd –: Intra-aortic Balloon Pump Market Study 2020-2029, that includes a comprehensive analysis of a range of subjects such as ...

Maquet/Datascope is recalling all intra-aortic balloon pumps (IABPs) after reports of the batteries failing to hold a charge, stopping unexpectedly, and having a shortened run-time, according to 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 ...

Some of the intra-aortic balloon pumps (IABP) made by Maquet Datascope Corporation were recalled in March 2014 because the device's fan assembly could malfunction and cause the device to stop with any ...

WAYNE, N.J., May 26, 2015 /PRNewswire/ -- Maquet Getinge Group announced today the publication of a manuscript describing the exploration of the hemodynamic effects of the newer, larger-capacity 50 cc ...

The FDA announced that Maquet Datascope Corp. has recalled a hybrid intra-aortic balloon pump due to a design issue that allows fluid, such as saline, to seep into the device. The agency designated ...

A Japanese study of intra-aortic balloon pumps appears to indicate the devices do little to improve outcomes for patients with acute cases and may increase the chances of death. In the registry study ...

Mahwah, NJ-- MAQUET Cardiovascular LLC, a leading provider of cardiovascular technologies, announced U.S. Food & Drug Administration (FDA) 510(k) clearance and CE mark today at the 2011 Transcatheter ...