Skip to content
Recall Observatory FDA recall evidence

Device product

LVP software of the Ivenix Infusion System (IIS); LVP-SW-0004

Z-1283-2024

May 10, 2023

Class II

Product summary

Firm
Fresenius Kabi USA, LLC
Event
Event 93968
Status
Completed
Classification
Class II
Quantity
6 US
Official record key
device-enforcement:Z-1283-2024

Official wording

Reason: Retroactively reported corrections from 2023: 1) A software defect may cause an incorrect (Fail-Stop) alarm when an administration set is loaded or coupled while the pump is executing the power-up sequence. May lead to delay in therapy. 2) Alert is not annunciated informing the clinician that the bolus cannot be delivered when the entered bolus dose exceeds the Care Profile Hard Rate Max limit and Rapid Bolus is selected. May lead to over infusion. Both issues were resolved in all fielded product in software version 5.8.0, which was installed in affected units May thru August 2023.

Code information: UDI-DI 00811505030122 Software versions 5.2.1/5.2.2

Distribution pattern: US Nationwide distribution to the states of CA, CO, NJ, WI, UT.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software defect may cause an incorrect