CardioQuip recalls MCH-1000(m) modular cooler-heaters due to potential bacterial contamination causing patient infections. Affected units have specific UDI and lot numbers.
“CardioQuip MCH-1000(m) Cooler-Heater Recall: Bacterial Contamination Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57011-cardioquip-mch-1000-m-cooler-heater-recall-bacterial-contamination-risk. Based on FDA recall #Z-0566-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0566-2024%22&limit=1).
CardioQuip, LLC voluntarily recalled its Modular Cooler-Heater, Model MCH-1000(m), due to potential bacterial contamination that could cause patient infection, the FDA said on Oct. 24, 2023.
How to tell if you have it
Brand: CardioQuip
Product: Modular Cooler-Heater
Model: MCH-1000(m)
Power: 115V-60Hz, 16A
UDI: 00860000846110
Lot #: 11160294 and 11161110
Quantity: 2 units
Sold in: California, Texas, Pennsylvania, Washington, Ohio, Nebraska
The hazard
The cooler-heater devices may contain bacterial contamination which could result in patient infection.
Context
GovInfoNow's records show CardioQuip, LLC has issued three other recalls since May 12, 2021, including a Oct. 19, 2023 recall for heating chamber melting risks and a June 24, 2021 recall for bacterial contamination. Other recent recalls of similar products include the ICU Medical Hotline Fluid Warming Set Recall (June 24, 2026), the Covidien Mon-a-Therm Temperature Probe Recall (April 23, 2026), and the Medtronic GUNDRY Cannula Recall (April 21, 2026).
How to tell if you have this one
Check for the model number MCH-1000(m) on the device. Affected units have UDI: 00860000846110 and lot numbers 11160294 or 11161110.
Brand
CardioQuip
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Identify the model number and UDI to confirm if your unit is affected.
Where it went and when
Where it was distributed
Distributed in 6 states.
Listed by the agency
Not listed
FDA distribution: “US: California, Texas, Pennsylvania, Washington, Ohio, Nebraska OUS: None” States read from FDA’s own wording; “not listed” means the notice does not name it.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0566-2024 (October 24, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0566-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.