Fresenius recalls AquaC UNO H medical devices with potential electrical shock hazard if ethernet port is touched due to misaligned internal cable. Affected units have specific serial numbers and part numbers.
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 is recalling AquaC UNO H medical devices that may have a misaligned internal ethernet cable. This could cause the cable's insulation to degrade at high temperatures, leading to electrical shock if the device's ethernet port is touched by service technicians or authorized operators.
The internal ethernet cable may become misaligned, causing its insulation to degrade under high temperatures. If the device's ethernet port is touched, this could allow electrical current to flow, resulting in electrical shock.
Service technicians and authorized operators using the AquaC UNO H medical device are most at risk. The recall affects specific units with the listed serial numbers and part numbers.
Check for the specific serial numbers listed in the recall notice (e.g., 2CHS5762, 1CHS5601) or the Vivonic part number G02000966-US. The device is sold as the AquaC UNO H [120V, 60Hz, 1700VA] with Fresenius US-Version: 24-0970-1.
If you are a service technician or authorized operator, stop using the AquaC UNO H device immediately to avoid electrical shock risk.
The recalled device is the AquaC UNO H [120V, 60Hz, 1700VA] with Fresenius US-Version: 24-0970-1 and Vivonic Part Number: G02000966-US.
Check your device's serial numbers against the list provided in the recall notice, which includes specific codes like 2CHS5762 and 1CHS5601.
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-1463-2022 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-1463-2022 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.
