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Recall Observatory FDA recall evidence

Device product

Ivenix Infusion System (IIS), LVP Software LVP-SW-0005. Indicated for use in a hospital and in outpatient care environments for the controlled administration of fluids through clinically accepted routes of administration.

Z-1019-2025

January 10, 2025

Class I

Product summary

Firm
Fresenius Kabi USA, LLC
Event
Event 96085
Status
Ongoing
Classification
Class I
Quantity
23 systems
Official record key
device-enforcement:Z-1019-2025

Official wording

Reason: Large Volume Pump Software, version 5.9.2 and earlier has potential for the following anomalies: 1. The pump may become nonfunctional if during an alarm condition the Pause Audio option is repeated 70 time or more. 2. If a secondary infusion is started at the exact moment a primary infusion completes and VTBI reaches 0, it will switch to primary. The primary infusion will infuse at the previously programed primary rate and continue until the infusion is stopped or the bag is empty.

Code information: UDI-DI: 00811505030122. Software 5.9.2 and prior

Distribution pattern: US distribution to CA, CO, GA, ID, MI, MS, NE, NJ, NV, OK, TX, UT, VA, WA, WI.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    Software, version 5.9.2 and earlier has potential for the following anomalies