---
title: "CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A — FDA record Z-0566-2024 | Is It on Recall"
description: "There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection."
url: https://isitonrecall.com/recall/fda-device-z-0566-2024-cardioquip-modular-cooler-heater-model-mch-1000-m-power-115v-60hz-16a/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A — FDA record Z-0566-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 24, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A
- **Reason**: There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.
- **Classification**: Class II
- **Recalling firm**: CardioQuip, LLC
- **Quantity**: 2 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0566-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0566-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI: 00860000846110 /Lot #:11160294 and 11161110 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US: California, Texas, Pennsylvania, Washington, Ohio, Nebraska OUS: None

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)
- [Nebraska](https://isitonrecall.com/state/nebraska/)
- [Ohio](https://isitonrecall.com/state/ohio/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Washington](https://isitonrecall.com/state/washington/)

## Dates in the source

- **Report date**: Dec 27, 2023
- **Recall initiation date**: Oct 24, 2023
- **Center classification date**: Dec 15, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0566-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [CardioQuip, LLC records](https://isitonrecall.com/brand/cardioquip-llc/)