Datascope Corporation: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Datascope Corporation in 2019. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Sensation Plus 7.5Fr. 40cc Intra-Aortic Balloon Catheter with accessories, Part Number 0684-00-0568-01 Product Usage: The Sensation Plus 7.5Fr. 40cc Intra-Aortic Balloon Catheter with accessories is a device that includes a catheter, an insertion kit and two STATLOCK IAB stabilization devices. It is a cardiac assist device intended to provide counterpulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the heart muscle and decreases the work of the left ventricle.