Use cautionMedical device recall · FDA · Published June 16, 2022
Fresenius AquaC UNO H: Risk of electrical shock from misaligned ethernet cable
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
Take action
Contact the company
📍Recalling firmFresenius Medical Care Holdings, Inc.920 Winter St Bld 950 · Waltham, MA 02451-1521
✎ GovInfoNow plain-language explainer
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. Read more at govinfonow.com/recall/60483-fresenius-aquac-uno-h-risk-of-electrical-shock-from-misaligned.
“Fresenius AquaC UNO H: Risk of electrical shock from misaligned ethernet cable.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60483-fresenius-aquac-uno-h-risk-of-electrical-shock-from-misaligned. Based on FDA recall #Z-1463-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1463-2022%22&limit=1).
The FDA announced on June 16, 2022, that Fresenius Medical Care Holdings, Inc. is recalling AquaC UNO H dialysis machines due to a risk of electrical shock. The hazard stems from an internal ethernet cable that may conduct current to the device's exterior port. Owners should contact the company for remedies.
How to tell if you have it
Brand: Fresenius
Product: AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 24-0970-1 Vivonic Part Number: G02000966-US
UPC: 04251285200234
Units affected: 277
The hazard
The internal ethernet cable may be misaligned, causing the cable jacket insulation to become compromised due to high temperature. This could result in the internal ethernet cable conducting electrical current to the ethernet port on the outside of the device. If the ethernet port is touched or manipulated, there is a risk of electrical shock potentially harming service technicians and/or other authorized operators.
Context
GovInfoNow's records show Fresenius Medical Care Holdings, Inc. has had 44 other recalls since April 14, 2014. Recent Fresenius recalls include a May 12, 2026, notice for Bicarby Dialysate leaks and a May 11, 2026, recall for 5008X Blood Tubing Set online port errors. Other recent recalls of similar products include GE Allia Moveo X-ray System Recall (April 20, 2026) and GE Medical Systems Allia IGS 3 Pulse X-Ray System Recall (April 20, 2026).
How to tell if you have this one
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.
Brand
Fresenius
Product
AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 24-0970-1 Vivonic Part Number: G02000966-US
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
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.
Official source: FDA Recall #Z-1463-2022 (June 16, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1463-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.