3 recalls found for Fresenius Kabi USA. Check if any of your products are affected.
Fresenius Kabi USA recalled 30 units of the Ivenix Infusion System LVP Software on November 21, 2025. The recall addresses concerns related to programming instructions for LVP duration. Patients and healthcare providers must stop using the device immediately.
Fresenius Kabi USA recalled 15,862 Ivenix Infusion Systems on November 3, 2025. The recall affects model LVP-0004 due to downstream occlusion alarms during low flow infusions. Healthcare providers and patients should stop using the device immediately.
Fresenius Kabi USA recalled 12,075 infusion pump administration sets on November 3, 2025. The recall stems from incorrect assembly that poses a serious risk of patient injury. Healthcare providers and patients should stop using the devices immediately.