Datascope Cardiosave Hybrid And Rescue Intra-aortic Balloon Pumps (iabp)

Recall Summary Datascope Cardiosave Hybrid and Rescue Intra-Aortic Balloon Pumps are being recalled in Canada due to performance issues. These medical devices are used to support heart function during cardiac procedures. The recall affects units distributed across Canada.

Product

Datascope Cardiosave Hybrid And Rescue Intra-Aortic Balloon Pumps (IABP)

Reason

Performance

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2023-06-16

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f7b7b8e1-9d96-4f2d-9cea-a6d7dea47e05