Cardiosave Intra-aortic Balloon Pump (iabp) (2018-05-08)

CARDIOSAVE Intra-Aortic Balloon Pump Recall The CARDIOSAVE Intra-Aortic Balloon Pump (IABP), a medical device used to support heart function, has been recalled across Canada. The specific reason for this Class I recall has not been detailed in the available information. This recall affects all units of this device that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-05-25
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/76eafb92-62ea-42c2-bd05-c5911c076243