FDAMay 10, 2023device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Completed

Brands named

fresenius kabifresenius

UPCs

00811505030122

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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