# FDA recall Z-0273-2022

> **Medtronic Perfusion Systems** · Class II · device recall initiated 2021-09-27.

## Product

Cardioblate CryoFlex Surgical Ablation Console

## Reason for recall

There is potential for intermittent electrical connectivity between the console and probe.

## Distribution

Distribution in US - IL, KS, and UT  Distribution outside of US to Australia and South Korea

## Key facts

- **Recall number:** Z-0273-2022
- **Recalling firm:** Medtronic Perfusion Systems
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-09-27
- **Report date:** 2021-12-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brooklyn Park, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0273-2022

## Citation

> AI Analytics. FDA recall Z-0273-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0273-2022. Source: US FDA. Licensed CC0.

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