Fresenius recalls AquaC UNO H hemodialysis reverse osmosis units due to missing ferrite cores in internal cables, affecting electromagnetic compatibility. No remedy specified in official notice.
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 reverse osmosis units because internal cables lack ferrite cores, which could cause electromagnetic interference. This may affect the unit's safety and performance during dialysis treatments.
The unit's internal cables are missing one or both ferrite cores, which are essential for managing electromagnetic interference. Without them, the device may not function properly with hemodialysis systems, potentially causing safety issues during treatment.
Hemodialysis patients using the AquaC UNO H units are most at risk. The recall applies to specific model numbers and serial numbers listed in the official notice.
Check for the model number 'AquaC UNO H [120V, 60Hz, 1700VA, US-Version' and serial numbers starting with 0CHS3987, 0CHS4108, 1CHS5372, 1CHS5405, 9CHS2881, or 9CHS3090.
Verify the model number and serial numbers listed in the official recall notice to confirm if your unit is affected.
The official recall notice does not specify any remedy for this issue.
The recall notice states no remedy is provided, so you should check the product details to see if your unit is affected.
Look for the model number 'AquaC UNO H [120V, 60Hz, 1700VA, US-Version' and serial numbers starting with 0CHS3987, 0CHS4108, 1CHS5372, 1CHS5405, 9CHS2881, or 9CHS3090.
We’ve drafted a message you can send Fresenius to request your refund or repair — edit it as you like.
Subject: Recall Z-1770-2022 — Fresenius Fresenius Hello, I own a Fresenius that is covered by recall Z-1770-2022 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.
