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# Fresenius Kabi Recalls Ivenix Infusion Software
- URL: https://www.fdaweb.com/fresenius-kabi-recalls-ivenix-infusion-software/
- Published: 2025-03-07T12:00:00.000Z
- Updated: 2026-09-14T14:54:51.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5158782

Fresenius Kabi USA has recalled its Ivenix LVP software, embedded in its Ivenix Infusion System, due to anomalies associated with software versions 5.9.2 and earlier. The anomalies have the potential to cause serious patient harm or death, a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/update-alert-infusion-pump-software-issue-fresenius-kabi-usa?ref=fdaweb.com) says. For example, if during an alarm mode and the “Pause Audio” option is repeated 70 times or more, it will result in the pump becoming nonfunctional, which may lead to the patient being underdosed, it says.