The FDA is issuing this update to inform the health care community of the final PAS results and updated labeling for the Impella RP System by Abiomed. Link to original article Getinge Maquet/Datascope Intra-Aortic Balloon Pump (IABP) Shortage - Letter to Health Care Providers Update on Risk of Type III Endoleaks with Use of Endologix AFX Endovascular AAA Graft Systems – FDA Safety Communication Share Print Please login or register to post comments.