CardioQuip recalls MCH-1000(i) cooler-heaters with potential heating chamber melting/burning. Affected units have specific serial numbers. Stop using immediately to prevent fire or injury.
There is a potential for the heating-chamber to malfunction resulting in melting/burning of the heater chamber components.
CardioQuip is recalling its MCH-1000(i) modular cooler-heater models due to a risk of the heating chamber melting or burning. This could cause fire or injury if the device is used as intended.
The heating chamber in these devices may malfunction, causing components to melt or burn. This could lead to fire or injury if the device is used normally without proper maintenance.
Owners of CardioQuip MCH-1000(i) cooler-heaters with the listed serial numbers are affected. People using these devices for home or commercial cooling/heating are most at risk.
Check the serial numbers listed in the recall notice. The affected models have specific serial numbers starting with 10160 and ending with various numbers.
Discontinue use of the device to prevent potential fire or injury from melting components.
The recalled model is CardioQuip MCH-1000(i) with specific serial numbers listed in the notice.
Check the serial number on your device against the list of affected serial numbers provided in the recall notice.
Stop using the device immediately to prevent potential fire or injury. Contact CardioQuip for further instructions.
We’ve drafted a message you can send CardioQuip to request your refund or repair — edit it as you like.
Subject: Recall Z-0439-2024 — CardioQuip CardioQuip Hello, I own a CardioQuip that is covered by recall Z-0439-2024 from CardioQuip. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
