Fresenius Kabi USA, LLC recalls Ivenix Infusion System (IIS), Large Volume Pump, Model No. LVP-0004

Recalled April 19, 2023 · FDA recall Z-1313-2023 · Fresenius Kabi USA

Hazard

Fluid ingress that can cause a loss of electrical funtion and failure of the Set ID Sensory, resulting in the prevention of infusion or halt of infusion. · FDA Class I

Units

1,546 units

Sold at

Domestic: CA, CO, NJ, WI, & UT. No foreign distribution.

Description

Fluid ingress that can cause a loss of electrical funtion and failure of the Set ID Sensory, resulting in the prevention of infusion or halt of infusion.

Product

Ivenix Infusion System (IIS), Large Volume Pump, Model No. LVP-0004

Manufacturer(s)

Fresenius Kabi USA, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →