CardioQuip recalls its Modular Cooler-Heater 1000(i) units due to missing water quality maintenance instructions. Owners should check serial numbers and follow official guidance to prevent improper use.
Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.
CardioQuip is recalling its Modular Cooler-Heater 1000(i) units because the product lacks clear instructions for water quality maintenance and device inspections. This could lead to improper use if owners don't follow the necessary steps.
The device requires specific water quality maintenance and regular inspections to function safely. Without proper guidance, users might not maintain the system correctly, potentially causing issues like poor water quality or device malfunction.
Owners of CardioQuip Modular Cooler-Heater 1000(i) units with serial numbers starting with (01) 00860000846127 are affected. People using these units for water cooling in homes or businesses may need to check maintenance.
Check for the model number MCH-10RMS on the unit. The serial number starts with (01) 00860000846127. These units were sold with the CE 2797 certification.
Look for the serial number starting with (01) 00860000846127 on the unit.
No, the recall does not require stopping use. The hazard is about missing maintenance instructions, not immediate safety risks.
Check if your unit has the model number MCH-10RMS and a serial number starting with (01) 00860000846127.
The recall does not specify a remedy, so no action is required beyond checking if your unit is affected.
We’ve drafted a message you can send CardioQuip to request your refund or repair — edit it as you like.
Subject: Recall Z-0036-2022 — CardioQuip CardioQuip Hello, I own a CardioQuip that is covered by recall Z-0036-2022 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.
