Fresenius Vial recalls Volumat MC Agilia Volumetric Infusion Pump model Z021135 software version 1.7 due to potential software malfunctions. Affected healthcare facilities must update software to prevent issues.
Fresenius Kabi initiated a mandatory software upgrade of the Volumat MC Agilia Volumetric Infusion Pump because it was designed to improve customer experience while preventing common software malfunctions.
Fresenius Vial is recalling Volumat MC Agilia Volumetric Infusion Pumps with model number Z021135 and software version 1.7. The recall is due to potential software malfunctions that could affect patient safety during medical treatments.
The pump's software version 1.7 may experience malfunctions that could impact patient safety during IV treatments. However, the recall is for a software update to improve stability and prevent issues, not a critical failure.
Healthcare professionals and facilities using the Volumat MC Agilia Volumetric Infusion Pump model Z021135 with software version 1.7 are affected. Those administering IV treatments to patients are most at risk.
Check for the model number Z021135 and software version 1.7 on the pump's label. The pump is used in healthcare facilities for administering IV treatments to patients.
Contact Fresenius Vial to get the latest software update for the Volumat MC Agilia Volumetric Infusion Pump model Z021135.
Fresenius Vial initiated a mandatory software upgrade to prevent common software malfunctions and improve patient safety.
The recall is for a software update to prevent potential malfunctions, not an immediate safety hazard. The pump is designed to be safe when used correctly.
Check for model number Z021135 and software version 1.7 on the pump's label. The pump is used in healthcare facilities for administering IV treatments.
We’ve drafted a message you can send Fresenius Vial to request your refund or repair — edit it as you like.
Subject: Recall Z-0362-2019 — Fresenius Vial Fresenius Vial Hello, I own a Fresenius Vial that is covered by recall Z-0362-2019 from Fresenius Vial. 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.
