Maquet Datascope Corp - Cardiac Assist Division recalls

Maquet Datascope Corp - Cardiac Assist Division has 14 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 7 Nov 2018. 6 are still ongoing. The most frequent reason is device malfunction.

Total recalls14since 2014
Last 12 months0reported
Class I1071% of total
Ongoing6latest 7 Nov 2018

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 10 71%Class II 4 29%Class III 0 0%

Why maquet datascope corp - cardiac assist division is recalled

By year

Ongoing maquet datascope corp - cardiac assist division recalls

6 active

All maquet datascope corp - cardiac assist division recalls, newest first

14 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS ICardiosave Rescue IABP recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionOtherNationwide
DeviceCLASS ICardiosave Hybrid IABP recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionOtherNationwide
DeviceCLASS ICardiosave Hybrid Intra-Aortic Balloon Pump (Iabp) recalledMaquet Datascope Corp - Cardiac Assist DivisionOther49 states
DeviceCLASS ICS 300 Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS ICS 100i Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS ICS 100 Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS ICS 100 Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS ICS 100i Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS ICS 300 Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS IICardiosave Hybrid Iabp and Cardiosave Rescue Iabp affected recalledMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS IICardiosave Hybrid and rescue IABP recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionOtherNationwide
DeviceCLASS IIMaquet Cardiosave Hybrid Intra-Aortic Balloon Pump (Iabp) recalledMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide
DeviceCLASS IICardiosave Intra-Aortic Balloon Pump recalled by Maquet Datascope CorpMaquet Datascope Corp - Cardiac Assist DivisionOtherNJ
DeviceCLASS IDatascope System 98/98xt, CS 100/CS100i recalledMaquet Datascope Corp - Cardiac Assist DivisionDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.