CardioQuip recalls MCH-1000(m) modular cooler-heaters due to potential bacterial contamination causing patient infections. Affected units have specific UDI and lot numbers.
There is the potential that cooler-heater devices may contain bacterial contamination which could result in patient infection.
CardioQuip is recalling its MCH-1000(m) modular cooler-heaters because they may contain bacteria that could infect patients. This is serious for medical use but does not affect home users.
The cooler-heaters may have bacterial contamination that could lead to patient infections if used in medical settings. This is a contamination risk specific to clinical environments.
Medical facilities using these devices are most at risk. Home users are not affected since this product is for clinical settings only.
Check for the model number MCH-1000(m) on the device. Affected units have UDI: 00860000846110 and lot numbers 11160294 or 11161110.
Identify the model number and UDI to confirm if your unit is affected.
No, this product is designed for medical facilities only and not for home use.
Check the model number and UDI to see if it's affected; no action is needed if it's not listed.
Look for the model number MCH-1000(m) and UDI: 00860000846110 with lot numbers 11160294 or 11161110.
We’ve drafted a message you can send CardioQuip to request your refund or repair — edit it as you like.
Subject: Recall Z-0566-2024 — CardioQuip CardioQuip Hello, I own a CardioQuip that is covered by recall Z-0566-2024 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.
