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Serious recall: Injury is possible or has been reported. Take action promptly.

Fresenius Medical Care Holdings, Inc. 2022-08-03 Health serious FDA
Health · FDA · Recall #FDA-Z-1463-2022

AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 24-0970-1 Vivonic Part Number:… Recall

Issued August 3, 2022 · Fresenius Medical Care Holdings, Inc.

In August 2022, Fresenius Medical Care Holdings, Inc. recalled the AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 24-0970-1 Vivonic Part Number:…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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

What you should do

  1. 1 Stop using AquaC UNO H [120V, 60Hz, 1700VA, Fresenius US-Version: 24-0970-1 Vivonic Part Number:… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Fresenius Medical Care Holdings, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Fresenius Medical Care Holdings, Inc.
Category
Health
Recall date
August 3, 2022
Units affected
Not reported
Sold at
US Nationwide distribution.
Recall number
FDA-Z-1463-2022
Made in
United States
Issuing agency
FDA

In context

  • Fresenius Medical Care Holdings, Inc. has 8 recalls in our database, including 1 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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