Datascope/Getinge is recalling certain Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pumps (IABPs) because the coiled cable connecting the display and base on some units may fail, ...
The US Food and Drug Administration (FDA) has alerted users of Datascope Corp/MAQUET’s Cardiosave hybrid intra-aortic balloon pump (IABP) to a “design issue” that enables fluids to leak into the ...
Getinge is informing about a global Class 1 recall for Cardiosave Hybrid, Cardiosave Rescue, CS300 and CS100 Intra-Aortic Balloon Pumps (IABP). This field correction is being conducted to ensure all ...
Getinge is once again under scrutiny from FDA related to the company’s cardiovascular devices. The agency today sent a letter to healthcare providers highlighting continued safety and quality concerns ...
On Nov. 29, Getinge posted a notification letter informing customers of a shortage of Maquet/Datascope intra-aortic balloon (IAB) catheters, new Cardiosave intra-aortic balloon pump (IABP) devices, ...
WAYNE, N.J.--(BUSINESS WIRE)--CARDIOSAVE ® IABP HYBRID & RESCUE was one of 14 medical innovations on display in front of thousands of healthcare providers and experts at the Premier healthcare ...
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