FDAMay 6, 2026device

Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004

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

The hazard

Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.

What to do

FDA enforcement status: Ongoing

Brands named

fresenius kabifresenius

UPCs

00811505030320

Recall history

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

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