FDA Recall: Software anomalies can cause serious harm or death

Company: Fresenius Kabi USA, LLC
Date of Enforcement Report: 12/16/2025
Class: I

PRODUCT

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Software for the controlled administration of fluids to patients.

Recall Number:

Z-0885-2026

REASON:

Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.

RECALLING FIRM/MANUFACTURER:

Z-0885-2026

VOLUME:

30 units

DISTRIBUTION:

US (Domestic) distribution: CA, CO, FL, GA, ID, IL, MD, MI, MN, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA & WI.

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

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