Fresenius Kabi recalls Ivenix Infusion System Large Volume Pump Model LVP-0004 due to potential pneumatic valve failure that may stop active infusions or prevent pump use. Affected units have specific serial numbers listed in the recall.
Potential pneumatic valve failure that may cause the LVP to stop an active infusion and/or could prevent the pump from being used.
Fresenius Kabi is recalling its Ivenix Infusion System Large Volume Pump (Model LVP-0004) because a potential pneumatic valve failure could stop an active infusion or prevent the pump from being used. This affects specific units with the listed serial numbers.
The pump's pneumatic valve may fail, causing it to stop an active infusion or become unable to function properly. This could lead to treatment interruptions for patients requiring continuous medication delivery.
Patients using this specific infusion pump model are affected. Healthcare providers who administer these pumps are at the highest risk due to the potential for interrupted treatments.
Check if your pump has the model number LVP-0004 and the listed serial numbers (e.g., 9233532106, 9233421830, etc.). The recall includes specific serial numbers provided in the official notice.
Verify your pump has model number LVP-0004 and one of the listed serial numbers.
Reach out to Fresenius Kabi USA, LLC for guidance on next steps if your pump is affected.
Yes, the pump may stop an active infusion or become unable to function, which could interrupt critical medication delivery.
Check if your pump has model number LVP-0004 and one of the specific serial numbers listed in the recall notice.
Contact Fresenius Kabi USA, LLC to get guidance on next steps for affected units.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-0763-2025 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-0763-2025 from Fresenius Kabi. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
