Fresenius Kabi USA, LLC: Medical Device Recall in 2024 - (Recall #: Z-1283-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 10, 2023

Date Posted: March 20, 2024

Recall Number: Z-1283-2024

Event ID: 93968

Reason for Recall:

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.

Status: Completed

Product Quantity: 6 US

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.

Voluntary or Mandated:

Voluntary: Firm initiated