CardioQuip recalls
CardioQuip has 9 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 27 Dec 2023. 9 are still ongoing. The most frequent reason is processing deviation.
Total recalls9since 2021
Last 12 months0reported
Class I00% of total
Ongoing9latest 27 Dec 2023
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 9 100%Class III 0 0%
Why cardioquip is recalled
Product types
By year
Ongoing cardioquip recalls
9 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Other | 6 states |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Other | 6 states |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Device Malfunction | 15 states |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Device Malfunction | 15 states |
| Device | CLASS II | Modular Cooler-Heater 1000(i), Standard Unit recalled by CardioQuip | CardioQuip | Processing Deviation | Nationwide |
| Device | CLASS II | Modular Cooler-Heater 1000(m),Compact Unit recalled by CardioQuip | CardioQuip | Processing Deviation | Nationwide |
All cardioquip recalls, newest first
9 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Other | 6 states |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Other | 6 states |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Device Malfunction | 15 states |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Device Malfunction | 15 states |
| Device | CLASS II | Modular Cooler-Heater 1000(i), Standard Unit recalled by CardioQuip | CardioQuip | Processing Deviation | Nationwide |
| Device | CLASS II | Modular Cooler-Heater 1000(m),Compact Unit recalled by CardioQuip | CardioQuip | Processing Deviation | Nationwide |
| Device | CLASS II | Modular Cooler-Heater 1000(m),Thermoelectric Cooling Lid recalled | CardioQuip | Processing Deviation | Nationwide |
| Device | CLASS II | Modular Cooler-Heater 1000(i), Refrigeration Module recalled | CardioQuip | Sterility | Nationwide |
| Device | CLASS II | Modular Cooler-Heater recalled by CardioQuip | CardioQuip | Processing Deviation | Nationwide |
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.