Maquet Datascope Corp - Cardiac Assist Division recalls

13 recalls on record · latest: September 20, 2018

Official U.S. recall history for Maquet Datascope Corp - Cardiac Assist Division, compiled from official government records.

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Maquet Datascope Corp - Cardiac Assist Division recalls Cardiosave Hybrid IABP, Part Number 0998-00-0800-53

September 20, 2018 · Medical device recalls High risk There is a potential for interruption and/or inability to start therapy to the…

Maquet Datascope Corp - Cardiac Assist Division recalls Cardiosave Rescue IABP, Part Number 0998-UC-0800-83

September 20, 2018 · Medical device recalls High risk There is a potential for interruption and/or inability to start therapy to the…

Maquet Datascope Corp - Cardiac Assist Division recalls CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding 0998-00-08…

May 3, 2018 · Medical device recalls High risk Ingress of fluids into the device can affect various electronic circuit boards…

Maquet Datascope Corp - Cardiac Assist Division recalls CS 100 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing…

July 17, 2017 · Medical device recalls High risk False blood back detection alarm and the ingress of fluids into the IABP affect…

Maquet Datascope Corp - Cardiac Assist Division recalls CS 100i Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing…

July 17, 2017 · Medical device recalls High risk False blood back detection alarm and the ingress of fluids into the IABP affect…

Maquet Datascope Corp - Cardiac Assist Division recalls CS 300 Intra-Aortic Balloon Pump. It supports the heart's left ventricle by increasing coronary perfusion and reducing…

July 17, 2017 · Medical device recalls High risk False blood back detection alarm and the ingress of fluids into the IABP affect…

Maquet Datascope Corp - Cardiac Assist Division recalls CS 300 Intra-Aortic Balloon Pump

June 16, 2017 · Medical device recalls High risk The device failed to pump due to an electrical test failure code #58 (power up…

Maquet Datascope Corp - Cardiac Assist Division recalls CS 100i Intra-Aortic Balloon Pump

June 16, 2017 · Medical device recalls High risk The device failed to pump due to an electrical test failure code #58 (power up…

Maquet Datascope Corp - Cardiac Assist Division recalls CS 100 Intra-Aortic Balloon Pump

June 16, 2017 · Medical device recalls High risk The device failed to pump due to an electrical test failure code #58 (power up…

Maquet Datascope Corp - Cardiac Assist Division recalls CARDIOSAVE Hybrid IABP and CARDIOSAVE Rescue IABP affected part number is 0998-:XX-0800-XX Li-Ion Battery affected part…

December 23, 2016 · Medical device recalls Moderate risk Maquet has received 3 confirmed complaints related to the Li-lon Battery used w…

Maquet Datascope Corp - Cardiac Assist Division recalls Cardiosave Hybrid and rescue IABP

December 16, 2015 · Medical device recalls Moderate risk Maquet has recieved information that in some Cardiosave IABPS, the scroll compr…

Maquet CARDIOSAVE Hybrid Intra-Aortic Balloon Pump recalled over fire hazard

January 30, 2015 · Medical device recalls Moderate risk Power supply malfunction complaints related to suboptimal thermal management.

Maquet Datascope Corp - Cardiac Assist Division product recalled over sterility concerns

December 16, 2014 · Medical device recalls Moderate risk Ferrule Cap was not removed on some fiber-optic Sensation and Sensation Plus IA…