Datascope/Getinge/Maquet Recalls Cardiosave Hybrid/Rescue Intra-Aortic Balloon Pump Battery Packs Due to Risk of Battery Failure

Date: 10/29/2021

Product type: Medical Device

• 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