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# Fresenius Recalls Ivenix Pump Administration Sets
- URL: https://www.fdaweb.com/fresenius-recalls-ivenix-pump-administration-sets/
- Published: 2024-09-16T12:00:00.000Z
- Updated: 2026-09-14T14:41:19.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157783

Fresenius Kabi is recalling (Class 1) one lot of the Ivenix Large Volume Pump (LVP) primary administration sets after documenting a manufacturing defect that may cause uncontrolled medication flow. “The use of affected product may cause serious adverse health consequences, including medication overdose and death,” a [recall notice](https://www.fda.gov/medical-devices/medical-device-recalls/infusion-pump-administration-set-recall-fresenius-kabi-usa-removes-certain-ivenix-large-volume-pump?utm%5Fmedium=email&utm%5Fsource=govdelivery) says. To date, there have been two reported injuries and no death reports.

The LVP uses air pressure to control the flow of fluids to patients. It is used in hospitals and outpatient centers to carefully give fluids to patients through different routes like IVs, in arteries, in the spine, or under the skin.