# FDA device recall: Ivenix Infusion System (IIS), Large Volume Pump, Model Number: LVP-0004

> recall · VERIFIED · 2026-05-06

Firm: Fresenius Kabi USA, LLC · Class I · Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the

- Company: Fresenius Kabi USA, LLC
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.