Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Battery Packs

Date: 21/09/2021

Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Battery Packs
Product Codes and Lot Numbers: See Recall Database Entry
Devices Recalled in the United States: 137 battery packs
Distribution Date: September 23, 2017 to August 17, 2021
Date Initiated by Firm: September 21, 2021

US-FDA Link: https://www.fda.gov/medical-devices/medical-device-recalls/datascopegetingemaquet-recalls-cardiosave-hybridrescue-intra-aortic-balloon-pump-battery-packs-due