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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 →