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# Fresenius Recall Infusion Pump Softeware
- URL: https://www.fdaweb.com/fresenius-recall-infusion-pump-softeware/
- Published: 2024-04-17T12:00:00.000Z
- Updated: 2026-09-14T14:28:30.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156800

Fresenius Kabi USA has recalled its Ivenix Infusion System’s pump software due to a necessary software update. “The reason for the recall is that multiple software anomalies were occurring that have the potential to result in serious patient harm or death,” a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/fresenius-kabi-usa-llc-recalls-ivenix-infusion-pump-lvp-software-anomalies-have-potential-cause?utm%5Fmedium=email&utm%5Fsource=govdelivery) says. “To remedy this issue, Fresenius Kabi is releasing a new software version (5.9.1) for the Ivenix Large Volume Pump (LVP).” To date, it says there have been no injury reports associated with the issue.

The pump is indicated for hospital use and in outpatient care environments for the controlled administration of fluids to patients through accepted methods such as intravenous line, arterial lines, epidurals, and subcutaneous delivery.