The FDA is alerting health care facilities and providers of a shortage of Getinge Maquet/Datascope Intra-Aortic Balloon Pump (IABP) devices, including limited supplies of IAB catheters, new Cardiosave IABPs, and Cardiosave IABP parts.Link to original article Getinge’s Maquet/Datascope IABP Devices: Update on Device Failure – Letter to Health Care Providers UPDATE: Impella RP System Post-Approval Study Results and Updated Labeling - Letter to Health Care Providers Share Print Please login or register to post comments.