Recall of Fresenius Kabi Ivenix Infusion System Large Volume Pump Model LVP-0004 due to fluid ingress causing electrical failure and infusion halt. Affected units have specific serial numbers listed in the recall notice.
Fluid ingress that can cause a loss of electrical funtion and failure of the Set ID Sensory, resulting in the prevention of infusion or halt of infusion.
Fresenius Kabi is recalling its Ivenix Infusion System Large Volume Pump (Model LVP-0004) because fluid can enter the device, causing electrical failure and stopping the infusion process. This could lead to treatment interruptions for patients using the pump.
Fluid ingress into the pump can cause electrical failure, which may prevent the pump from functioning properly. This could result in the infusion process being halted, potentially interrupting critical treatment for patients.
Patients using this specific infusion pump model are affected. Those with the listed serial numbers are most at risk as the pump may stop delivering medication or fluids during treatment.
Check the serial number on the pump's label. Affected units have specific serial numbers listed in the recall notice, including 2118200008, 2118200011, and many others.
Look for the serial number on the pump's label to determine if it's affected. Affected units have specific serial numbers listed in the recall notice.
Reach out to Fresenius Kabi for further instructions on how to address the issue if your pump is affected.
The recalled model is Ivenix Infusion System Large Volume Pump, Model No. LVP-0004.
Check the serial number on the pump's label. Affected units have specific serial numbers listed in the recall notice, including 2118200008, 2118200011, and many others.
Contact Fresenius Kabi for further instructions on how to address the issue if your pump is affected.
We’ve drafted a message you can send Fresenius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-1313-2023 — Fresenius Kabi Fresenius Kabi Hello, I own a Fresenius Kabi that is covered by recall Z-1313-2023 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.
