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Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Recalled January 15, 2025 · FDA recall Z-0763-2025 · Fresenius Kabi USA
Hazard
Potential pneumatic valve failure that may cause the LVP to stop an active infusion and/or could prevent the pump from being used. · FDA Class I
Units
1,520 units
Sold at
US distribution to states of: ID, MN, NV, TX, VA, WI.
Description
Potential pneumatic valve failure that may cause the LVP to stop an active infusion and/or could prevent the pump from being used.
Product
Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004
Manufacturer(s)
Fresenius Kabi USA, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →