Cardioblate CryoFlex Surgical Ablation Console
Reported: December 1, 2021 Initiated: September 27, 2021 #Z-0273-2022
Product Description
Cardioblate CryoFlex Surgical Ablation Console
Reason for Recall
There is potential for intermittent electrical connectivity between the console and probe.
Details
- Recalling Firm
- Medtronic Perfusion Systems
- Units Affected
- 7 devices
- Distribution
- Distribution in US - IL, KS, and UT Distribution outside of US to Australia and South Korea
- Location
- Brooklyn Park, MN
Frequently Asked Questions
What product was recalled? ▼
Cardioblate CryoFlex Surgical Ablation Console. Recalled by Medtronic Perfusion Systems. Units affected: 7 devices.
Why was this product recalled? ▼
There is potential for intermittent electrical connectivity between the console and probe.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 1, 2021. Severity: Moderate. Recall number: Z-0273-2022.
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