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Medical Device

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

Recall date: 2026-06-10 · Source: FDA_DEVICE
Brand / Firm
Fresenius Kabi USA, LLC
Product
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
Reason for recall
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.
Units affected
32 systems
Description
LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.
View official recall notice →