CardioQuip recalls specific MCH-1000(m) cooler-heaters due to potential heating chamber melting/burning. Affected units have listed serial numbers. No remedy stated in official notice.
There is a potential for the heating-chamber to malfunction resulting in melting/burning of the heater chamber components.
CardioQuip is recalling certain MCH-1000(m) modular cooler-heaters that could melt or burn due to heating chamber malfunction. This poses a fire risk if the device overheats.
The heating chamber in these devices may malfunction and overheat, causing components to melt or burn. This could lead to fire or injury if the device is left unattended or in a confined space.
Owners of the specific MCH-1000(m) models with listed serial numbers are affected. Users in environments where the device is plugged in and operating are most at risk.
Check for the model MCH-1000(m) with power rating 115V-60Hz,16A. Affected units have serial numbers listed in the official recall notice.
Verify the model number and serial number against the list provided in the recall notice.
The official recall notice does not state any remedy for this issue.
Check if your unit has the model MCH-1000(m) and a serial number from the list provided in the recall notice.
The official recall notice does not specify any action steps for affected units.
We’ve drafted a message you can send CardioQuip to request your refund or repair — edit it as you like.
Subject: Recall Z-0438-2024 — CardioQuip CardioQuip Hello, I own a CardioQuip that is covered by recall Z-0438-2024 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.
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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.
