Fresenius Kabi recalls Ivenix Infusion System software over ‘anomalies’
Large volume infusion pump software related to the Ivenix Infusion System has been recalled by its manufacturer due to multiple potentially dangerous issues, according to a press release from the FDA. The FDA classified the recall by Fresenius Kabi USA as a class 1 recall, meaning use of the devices “may cause serious injuries or death.” No injuries or deaths associated with the