CardioQuip recalls its MCH-1000(m) modular cooler-heater units due to missing water quality maintenance instructions. Owners should check serial numbers and contact the company for details.
Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.
CardioQuip is recalling its MCH-1000(m) modular cooler-heater units because the product lacks clear instructions for water quality maintenance and device inspections. This could lead to improper use if users don't follow necessary maintenance steps.
The device requires specific water quality maintenance and regular inspections to function safely. Without clear labeling, users might not know how to maintain the unit, potentially causing issues like poor water quality or device malfunction.
Owners of CardioQuip MCH-1000(m) modular cooler-heater units with serial numbers listed in the recall. People using these units for home or commercial water cooling are most at risk if they don't maintain the device properly.
Check the serial number on your CardioQuip MCH-1000(m) unit. The recall covers all units with the serial numbers listed in the official notice.
Look for the serial number on your CardioQuip MCH-1000(m) unit to confirm if it is affected.
No, the recall does not require stopping use. The issue is about missing labeling for maintenance, not immediate safety risks.
Check the serial number on your unit. All CardioQuip MCH-1000(m) units are affected by this recall.
The recall does not specify a remedy, so contact CardioQuip directly for guidance on maintenance steps.
We’ve drafted a message you can send CardioQuip to request your refund or repair — edit it as you like.
Subject: Recall Z-0037-2022 — CardioQuip CardioQuip Hello, I own a CardioQuip that is covered by recall Z-0037-2022 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.
