Fresenius Kabi is recalling the Ivenix Large Volume Pump (LVP), a primary component of the Ivenix Infusion System, because some units have mechanical issues with the Fluid Valve Pins, located inside the pump’s internal housing, causing the pins to not move properly.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
