Maquet Datascope Corp - Cardiac Assist Division: Medical Device Recalls in 2015

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Maquet Datascope Corp - Cardiac Assist Division in 2015. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP)
CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for human use, SENSATION and SENSATION PLUS IABC demonstration units. Part Number 0998-00-0800-xx; 0998-00-3023-xx; 0998-UC-0800-xx; 0998-UC-3023-xx An electromechanical system used to inflate and deflate intra-aortic balloons.