# FDA recall Z-0439-2024

> **CardioQuip, LLC** · Class II · device recall initiated 2023-10-19.

## Product

CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A

## Reason for recall

There is a potential for the heating-chamber to malfunction resulting in melting/burning of the heater chamber components.

## Distribution

US Distribution: TX, IN, IL, WI, FL, NJ, PA, KY, VA, WV, CT, CA, WA, AL, IA

## Key facts

- **Recall number:** Z-0439-2024
- **Recalling firm:** CardioQuip, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-19
- **Report date:** 2023-12-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** College Station, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0439-2024

## Citation

> AI Analytics. FDA recall Z-0439-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0439-2024. Source: US FDA. Licensed CC0.

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