Cs300, Cs100, Cardiosave Hybrid, And Cardiosave Rescue Iabp (2019-07-02)

Recall Summary Abiomed is recalling four intra-aortic balloon pump (IABP) models—CS300, CS100, Cardiosave Hybrid, and Cardiosave Rescue—across Canada due to a device malfunction issue. These are heart support devices used in medical settings to assist circulation in patients with heart problems. The recall affects all units of these models that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-07-09

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5c7f5eb9-5194-407e-a5b9-f71b5ed30618