Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cardioblate CryoFlex Surgical Ablation Console Recalled by Medtronic Perfusion Systems Due to There is potential for intermittent electrical connectivity between...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Perfusion Systems directly.
Affected Products
Cardioblate CryoFlex Surgical Ablation Console
Quantity: 7 devices
Why Was This Recalled?
There is potential for intermittent electrical connectivity between the console and probe.
Where Was This Sold?
This product was distributed to 3 states: IL, KS, UT
About Medtronic Perfusion Systems
Medtronic Perfusion Systems has 96 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report