---
title: "CardioQuip, LLC Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall"
description: "Search CardioQuip, LLC recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions."
url: https://isitonrecall.com/brand/cardioquip-llc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Home](https://isitonrecall.com/) / Brand archive

# CardioQuip, LLC recall records

**4** reported ongoing

4 records in this archive. Latest source date Oct 24, 2023.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

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/).

## Records and reported status

Oct 24, 2023 FDA device enforcement

### [CardioQuip Modular Cooler-Heater, Model: MCH-1000(i), Power: 115V-60Hz, 16A](https://isitonrecall.com/recall/fda-device-z-0565-2024-cardioquip-modular-cooler-heater-model-mch-1000-i-power-115v-60hz-16a/)

There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.

Class II Reported ongoing

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

[Official source for CardioQuip Modular Cooler-Heater, Model: MCH-1000(i), Power: 115V-60Hz, 16A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0565-2024%22)

Oct 24, 2023 FDA device enforcement

### [CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A](https://isitonrecall.com/recall/fda-device-z-0566-2024-cardioquip-modular-cooler-heater-model-mch-1000-m-power-115v-60hz-16a/)

There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.

Class II Reported ongoing

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

[Official source for CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0566-2024%22)

Oct 19, 2023 FDA device enforcement

### [CardioQuip Modular Cooler-Heater, Model:MCH-1000(m), Power: 115V-60hz,16A](https://isitonrecall.com/recall/fda-device-z-0438-2024-cardioquip-modular-cooler-heater-model-mch-1000-m-power-115v-60hz-16a/)

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

Class II Reported ongoing

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

[Official source for CardioQuip Modular Cooler-Heater, Model:MCH-1000(m), Power: 115V-60hz,16A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0438-2024%22)

Oct 19, 2023 FDA device enforcement

### [CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A](https://isitonrecall.com/recall/fda-device-z-0439-2024-cardioquip-modular-cooler-heater-model-mch-1000-i-power-115v-60hz-16a/)

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

Class II Reported ongoing

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

[Official source for CardioQuip Modular Cooler-Heater, Model:MCH-1000(i), Power: 115V-60hz,16A](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0439-2024%22)

## Reasons in these listed records

- There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.
- There is a potential for the heating-chamber to malfunction resulting in melting/burning of the heater chamber components.

These examples come from this result page and are not a ranking of every recall reason.

## Checking CardioQuip, LLC

### Is there a recall on cardioquip, llc right now?

This archive contains 4 records, including 4 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

### How do I check my package or product?

Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier.

### Does a matching name mean every item is included?

A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall.

### What if the search finds no matching record?

This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices.

### Where can I find older records?

Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

## Keep checking

[Search CardioQuip, LLC](https://isitonrecall.com/check/?q=CardioQuip%2C%20LLC) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)
