# FDA recall Z-1464-2022

> **Fresenius Medical Care Holdings, Inc.** · Class II · device recall initiated 2022-06-16.

## Product

AquaC UNO H [120V, 60Hz, 1000VA,  Fresenius US-Version:   24-10VA-1 Vivonic Part Number:  G02000970-US

## Reason for recall

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

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1464-2022
- **Recalling firm:** Fresenius Medical Care Holdings, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-06-16
- **Report date:** 2022-08-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waltham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1464-2022

## Citation

> AI Analytics. FDA recall Z-1464-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1464-2022. Source: US FDA. Licensed CC0.

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