CardioQuip recalls MCH-1000(i) 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(i) 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 the MCH-1000(i) model are most at risk. Home users are not affected by this recall.
Check for the model MCH-1000(i) with power 115V-60Hz, 16A. Affected units have UDI numbers starting with 00860000846103 and lot numbers 10161316, 10161479, 10160241, or 10161040.
Identify the model number, power specifications, and UDI/lot numbers to confirm if your unit is affected.
The recall is due to potential bacterial contamination in the cooler-heaters that could result in patient infections.
No, home users are not affected by this recall as it is specific to medical facilities.
The recall does not specify a remedy, so medical facilities should contact CardioQuip directly for guidance.
We’ve drafted a message you can send CardioQuip to request your refund or repair — edit it as you like.
Subject: Recall Z-0565-2024 — CardioQuip CardioQuip Hello, I own a CardioQuip that is covered by recall Z-0565-2024 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.
