Fresenius Kabi recalls Ivenix Large Volume Pump (LVP-0004) due to potential downstream occlusion alarms during low flow infusions with check valves added to the administration set.
Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.
Fresenius Kabi is recalling its Ivenix Infusion System Large Volume Pump (model LVP-0004) because adding a check valve to the administration set can trigger downstream occlusion alarms during low flow infusion rates. This could lead to incorrect infusion rates or treatment interruptions for patients using the pump.
When a check valve is added to the Ivenix Administration Set during low flow infusion rates, the system may trigger downstream occlusion alarms. This can cause incorrect infusion rates or treatment interruptions, potentially affecting patient safety.
Healthcare professionals using the Ivenix Large Volume Pump (model LVP-0004) with check valves added to the administration set are affected. Patients receiving infusions through this system are at risk if the check valve is used incorrectly.
Check for the model number LVP-0004 on the Ivenix Infusion System Large Volume Pump. The product was sold with a check valve added to the administration set during procedures.
Ensure the check valve is not added to the Ivenix Administration Set when using low flow infusion rates.
The recall is due to potential downstream occlusion alarms occurring during low flow infusions when a check valve is added to the administration set.
The affected model number is LVP-0004 for the Ivenix Infusion System Large Volume Pump.
The official recall does not provide a specific fix; users must ensure the check valve is not added to the administration set during low flow infusions.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-0848-2026 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-0848-2026 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.
