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,

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,