Home / Recalls / Medical Devices
Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.
Recalled January 21, 2026 · FDA recall Z-1048-2026 · Fresenius Kabi USA
Hazard
Emphasizing instructions for LVP duration programming located in the IFU. · FDA Class II
Units
30 units
Sold at
US Nationwide distribution in the states of CA, CO, FL, GA, ID, IL, MD, MI, MI, MN, MS, NE, NJ, NV, OK, OR, SC, TX, VA, WA, WI, WI.
Description
Emphasizing instructions for LVP duration programming located in the IFU.
Product
Ivenix Infusion System (IIS), LVP Software: LVP-SW-0005.
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →