FDAMay 6, 2026device

LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.

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

The hazard

Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to AC mains power.

What to do

FDA enforcement status: Ongoing

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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LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005. — Recall Details · AllClear