# FDA device recall: LVP software of the Ivenix Infusion System (IIS); Product Code LVP-SW-0005.

> recall · VERIFIED · 2026-05-06

Firm: Fresenius Kabi USA, LLC · Class I · Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless it is reconnected to

- 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.