Fresenius Kabi USA, LLC: Medical Device Recalls in 2024
Updated on March 25, 2026.
According to to data from the FDA, there were 5 medical device recalls made by Fresenius Kabi USA, LLC in 2024. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Ivenix Infusion System (IIS), LVP Software; LVP-SW-0004, Software Version 5.9.1 and prior. Infusion pump software for infusion management system.
- LVP software of the Ivenix Infusion System (IIS); LVP-SW-0004
- LVP software of the Ivenix Infusion System (IIS), LVP-SW-0004
- LVP Software of the Ivenix Infusion System (IIS), Version 5.8.0.
- LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25), Product Code: SET-0013-25. for intravenous infusion.
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