ClearanceBrief
Recall Z-2616-2021 ยท DSP System, Balloon, Intra-Aortic And Control

Datascope Corp.

Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85

DateSep 8, 2021
StatusOpen, Classified
ReasonThe Cardiosave IABP may unexpectedly shut down when the device is running on AC power, only one battery is installed in the IABP, and the battery is physically removed while the battery is being charged. This occurs during a very specific set of conditions.
Root causeSoftware design
ActionOn Wednesday, September 8, 2021, the firm distributed Urgent Medical Device Correction letters to affected customers. Customers were informed that all lots of Maquet Cardiosave Hybrid experience the following issue: Unexpected Shutdown Upon Battery Removal. Immediate Actions to be taken by Customers: To ensure that the Cardiosave Hybrid is not susceptible to shutdown during the removal of a battery, users should not eject a battery when: - There is a singulat battery in either battery charging bay and unused battery bay is empty. - The battery is charging on AC power (indicated by a flashin
Quantity3969 total (US); 3550 total (OUS)
DistributionNationwide domestic distribution. Foreign distribution worldwide.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K181122CARDIOSAVE Intra-Aortic Balloon Pump
Datascope Corp., May 31, 2018