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Maquet Datascope Corp - Cardiac Assist Division Recalls

9 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Maquet Datascope Corp - Cardiac Assist Division.

9Total Recalls
7Critical
57,885Units Affected
Sep 20, 2018Most Recent
All Recalls

Every Maquet Datascope Corp - Cardiac Assist Division Recall

Sorted by most recent. Click any recall for full details.

9 recalls
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
Cardiosave Hybrid IABP, Part Number 0998-00-0800-53
Medical Devices·0 affected·Sep 20, 2018
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
Cardiosave Rescue IABP, Part Number 0998-UC-0800-83
Medical Devices·0 affected·Sep 20, 2018
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding 0998-00-0800-83, 0998-UC-080...
Medical Devices·4,300 affected·May 3, 2018
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
CS 100 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing left ventricula...
Cardiac Devices·14,547 affected·Jul 17, 2017
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
CS 300 Intra-Aortic Balloon Pump
Medical Devices·12,319 affected·Jun 16, 2017
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
CS 100i Intra-Aortic Balloon Pump
Medical Devices·12,319 affected·Jun 16, 2017
CriticalFDA
Maquet Datascope Corp - Cardiac Assist Division
CS 100 Intra-Aortic Balloon Pump
Medical Devices·12,319 affected·Jun 16, 2017
High RiskFDA
Maquet Datascope Corp - Cardiac Assist Division
Cardiosave Hybrid and rescue IABP
Medical Devices·1,243 affected·Dec 16, 2015
High RiskFDA
Maquet Datascope Corp - Cardiac Assist Division
CARDIOSAVE Intra-Aortic Balloon Pump and CS300 Intra-Aortic Balloon Pump; and, non-sterile, not for human use, SENSATION and SENSATION PL...
Medical Devices·838 affected·Dec 16, 2014