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 monthSeverity split
Class I 10 71%Class II 4 29%Class III 0 0%
Why maquet datascope corp - cardiac assist division is recalled
Product types
By year
Ongoing maquet datascope corp - cardiac assist division recalls
6 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS I | Cardiosave Rescue IABP recalled by Maquet Datascope Corp | Maquet Datascope Corp - Cardiac Assist Division | Other | Nationwide |
| Device | CLASS I | Cardiosave Hybrid IABP recalled by Maquet Datascope Corp | Maquet Datascope Corp - Cardiac Assist Division | Other | Nationwide |
| Device | CLASS I | Cardiosave Hybrid Intra-Aortic Balloon Pump (Iabp) recalled | Maquet Datascope Corp - Cardiac Assist Division | Other | 49 states |
| Device | CLASS I | CS 300 Intra-Aortic Balloon Pump recalled by Maquet Datascope Corp | Maquet Datascope Corp - Cardiac Assist Division | Device Malfunction | Nationwide |
| Device | CLASS I | CS 100i Intra-Aortic Balloon Pump recalled by Maquet Datascope Corp | Maquet Datascope Corp - Cardiac Assist Division | Device Malfunction | Nationwide |
| Device | CLASS I | CS 100 Intra-Aortic Balloon Pump recalled by Maquet Datascope Corp | Maquet Datascope Corp - Cardiac Assist Division | Device Malfunction | Nationwide |
All maquet datascope corp - cardiac assist division recalls, newest first
14 totalAbout 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.