medical MODERATE Updated 2026-06-10

Fresenius Kabi USA, LLC recalls The Large Volume Pump (LVP) of the Ivenix Infusion System (I

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Recalled Product

The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS). Model Number: LVP-0004.

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Hazard / Issue

Potential for the Cassette Loading Lever to break.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model Number: LVP-0004. UDI-DI: 00811505030320

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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