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# Fresenius Recalls Ivenix Infusion Pump
- URL: https://www.fdaweb.com/fresenius-recalls-ivenix-infusion-pump/
- Published: 2022-10-07T12:00:00.000Z
- Updated: 2026-09-14T18:02:16.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5152925

Fresenius Kabi has recalled its Ivenix Infusion System’s large volume pump software due to a software design issue. A [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=196036&ref=fdaweb.com) says the display screen may become “frozen and unresponsive to user input, triggering an alarm that is evidenced by a buzzer sound and flashing red LEDs as a secondary notification.” It says that as the screen goes blank, it does not respond or indicate an alarm condition, which “leads to temporary cessation of flow of a medication or fluid, requiring immediate intervention by the clinician.” The company has notified customers about how to restart the device and obtain updated software that corrects the issue.