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Medtronic Perfusion Systems recalls Cardioblate CryoFlex Surgical Ablation Console
Recalled December 1, 2021 · FDA recall Z-0273-2022 · Medtronic Perfusion Systems
Hazard
There is potential for intermittent electrical connectivity between the console and probe. · FDA Class II
Units
7 devices
Sold at
Distribution in US - IL, KS, and UT Distribution outside of US to Australia and South Korea
Description
There is potential for intermittent electrical connectivity between the console and probe.
Product
Cardioblate CryoFlex Surgical Ablation Console
Manufacturer(s)
Medtronic Perfusion Systems
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →