Datascope Corp. Intra Aortic Balloon Pump (2017-07-20)

Recall Summary Datascope Corp. is recalling Intra Aortic Balloon Pump devices distributed across Canada due to a medical device issue. This Class I recall indicates a serious problem that could cause harm. The 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

2017-07-28

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d1b79eee-130c-498c-b6ed-29ebc5ec7324