Fresenius Kabi Issues Correction for Ivenix Infusion Pumps Following Impact Damage
The Food and Drug Administration classifies the recall as the most serious type after reports of touchscreen malfunctions caused by dropped or jarred devices.
The Food and Drug Administration classifies the recall as the most serious type after reports of touchscreen malfunctions caused by dropped or jarred devices.
Fresenius Kabi has issued an urgent recall of its Ivenix Large Volume Pump (LVP) for mechanical issues with the fluid valve pins.
A petition was submitted to the FDA to issue a corrective recall requiring modifications to dialysis machines manufactured by Fresenius.
The Food and Drug Administration classifies the recall as the most serious type after reports of touchscreen malfunctions caused by dropped or jarred devices.