Fresenius recalls AquaC UNO H hemodialysis units with missing ferrite cores in ethemet cables, risking electromagnetic interference. Affected units have specific serial numbers and part numbers.
Internal ethemet cables are missing one or both ferrite cores therefore the electromagnetic compatibility of the device is not ensured
Fresenius is recalling AquaC UNO H hemodialysis units that have missing ferrite cores in their internal cables. This could cause electromagnetic interference, which might affect the device's safety during dialysis treatments.
The device's internal ethernet cables lack one or both ferrite cores, which are essential for managing electromagnetic interference. Without them, the unit may not function properly with hemodialysis systems, potentially causing electrical issues during treatment.
Hemodialysis patients using the AquaC UNO H units with missing ferrite cores are most at risk. The recall affects specific units identified by serial numbers and part numbers.
Check for the serial numbers listed: 1CHS5379, 6CHS1192, 6CHS1194, and other specific numbers in the product description. The units also have Fresenius Part Number 24-10VA-1 and Vivonic Part Number G02000970-US.
Look for the serial numbers listed in the product description: 1CHS5379, 6CHS1192, 6CHS1194, and others.
The AquaC UNO H units have missing ferrite cores in their internal ethernet cables, which can affect electromagnetic compatibility with hemodialysis systems.
Check the serial numbers listed in the product description to see if your unit is affected. If it is, contact Fresenius for further instructions.
The issue could cause electromagnetic interference, which might affect the device's safety during dialysis treatments, but the recall indicates low risk.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-1769-2022 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-1769-2022 from Fresenius. 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.
