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Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004.
Recalled November 5, 2025 · FDA recall Z-0378-2026 · Fresenius Kabi USA
Hazard
Potential issue that can cause the device to register "phantom" touches in the lower-left corner of the touchscreen during operation. · FDA Class II
Units
6 units
Sold at
US Nationwide distribution in the state of Minnesota.
Description
Potential issue that can cause the device to register "phantom" touches in the lower-left corner of the touchscreen during operation.
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 →