Getinge/Datascope/Maquet Recalls Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Due to Reports of Fluid Leaks

Date: 01/05/2022

Product type: Medical Device

Product Names: Datascope/Getinge/Maquet Cardiosave Hybrid and Cardiosave Rescue Intra-Aortic Balloon Pump (IABP)
Manufacturing Dates: December 2011 to Present
Model Numbers: See Links to Recall Database Below
Distribution Dates: March 6, 2012 to October 21, 2021
Devices Recalled in the U.S.: 4,338
Date Initiated by Firm: October 27, 2021

USA-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/getingedatascopemaquet-recalls-cardiosave-hybrid-and-cardiosave-rescue-intra-aortic-balloon-pump