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Recall Observatory FDA recall evidence

Device product

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

Z-2224-2026

May 06, 2026

Class I

Product summary

Firm
Fresenius Kabi USA, LLC
Event
Event 98945
Status
Ongoing
Classification
Class I
Quantity
18,444
Official record key
device-enforcement:Z-2224-2026

Official wording

Reason: 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.

Code information: Model Number: LVP-0004; UDI-DI: 00811505030320; All Serial/Lot Numbers:

Distribution pattern: Domestic: CA, CO, FL, GA, ID, IL, MD, MI, MI , MN, MO, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA, WI, WI;

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.