Z-2224-2026 Class I Ongoing

Recalled by Fresenius Kabi USA, LLC — North Andover, MA

Recall Details

Product Type
Devices
Report Date
June 10, 2026
Initiation Date
May 6, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
18,444

Product Description

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

Reason for Recall

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.

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;

Code Information

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