Fresenius Kabi recalls Ivenix Infusion System over leaks that delay, interrupt therapy

The Ivenix Infusion System has been recalled by its manufacturer due to a system leak that may compromise the ability of the equipment to properly deliver infusions, according to press release from the FDA.The FDA classified the recall by Fresenius Kabi USA as a class 1 recall, indicating that continued use of the recalled devices “may cause serious injuries or death.”The Ivenix Infusion System model LVP-0004, a large volume pump used in health care settings to administer fluids to patients in controlled infusion amounts, was distributed from Oct. 27, 2021, through Jan. 30, 2023,Read More

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