Fresenius Kabi recalls Ivenix LVP-0004 infusion pumps that may malfunction after drops or jarring, causing random touchscreen inputs. Affected units have specific model and serial numbers.
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or readily visible and the devices therefore remained in service. More specifically, drops or jarring on a hard surface can cause the touchscreen input cable to loosen, resulting in unintended touchscreen behavior on the LVP, including random screen touches and/or lack of screen responsiveness to user input. Under the reported failure condition, unintended touch inputs may register at arbitrary screen locations without user interaction. These inputs occur intermittently and without a predictable pattern.
Fresenius Kabi is recalling Ivenix Large Volume Pumps (model LVP-0004) because drops or jarring can cause touchscreen issues. This may lead to unintended touches or unresponsive screens, which could affect patient safety during medical treatments.
Drops or severe jarring on hard surfaces can loosen the touchscreen cable inside the pump. This causes random touchscreen inputs or unresponsiveness, which might lead to incorrect medical settings during treatment.
Patients using Ivenix LVP-0004 infusion pumps for medical treatments are most at risk. The recall applies to specific model numbers and serial/lot numbers.
Check for model number LVP-0004 on the pump. Affected units have specific serial or lot numbers listed in the recall notice.
Look for the model number LVP-0004 on the pump's label.
Reach out to Fresenius Kabi USA for specific serial/lot numbers and next steps.
Drops or severe jarring can cause the touchscreen cable to loosen, leading to random touchscreen inputs or unresponsiveness.
Unintended touches or unresponsive screens may occur, which could affect medical treatment settings.
Check for model number LVP-0004 and specific serial/lot numbers listed in the recall notice.
We’ve drafted a message you can send Fresen:ius Kabi to request your refund or repair — edit it as you like.
Subject: Recall Z-2224-2026 — Fresen:ius Kabi Fresen:ius Kabi Hello, I own a Fresen:ius Kabi that is covered by recall Z-2224-2026 from Fresen:ius 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.
