The United States Food and Drug Administration (FDA) has revealed that Getinge subsidiary Datascope is recalling specific Cardiosave intra-aortic balloon pumps (IABPs) due to an increased likelihood of the devices ceasing operation without warning. The unplanned shutdowns result from communication problems between the device's … [Read more...] about Cardiosave Hybrid IABP and Cardiosave Rescue IABP Heart Devices Recalled for the Third Time in 2023