Fresenius Medical Care recalls AquaC UNO H devices with specific serial numbers due to potential electrical shock risk from misaligned internal ethernet cables. Affected units may cause harm to service technicians if the ethernet port is touched.
Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical current to the ethernet port on the outside of the device), potentially harming service technicians and/or other authorized operators. If the ethernet port on the device is touched or manipulated, there is a risk of electrical shock
Fresenius Medical Care is recalling AquaC UNO H medical devices because an internal ethernet cable may become misaligned, risking electrical shock if the port is touched by service technicians. This could harm authorized operators during maintenance.
The internal ethernet cable's insulation can become compromised due to high temperatures, potentially allowing electrical current to flow to the external ethernet port. If this port is touched, there is a risk of electrical shock to service technicians or authorized operators.
Service technicians and authorized operators using the AquaC UNO H devices with specific serial numbers listed in the recall. The risk is highest for those handling the device during maintenance.
Check if your AquaC UNO H device has a serial number starting with '8CHS' or '7CHS' or '2CHS' or '0CHS' as listed in the detailed serial numbers provided in the recall notice.
If you are a service technician or authorized operator, stop using the device immediately to avoid electrical shock risk.
The product is the AquaC UNO H medical device.
The recall includes specific serial numbers starting with '8CHS', '7CHS', '2CHS', or '0CHS' as listed in the detailed serial numbers provided in the recall notice.
The recall record does not mention any remedy or fix for this issue.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-1464-2022 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-1464-2022 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.
