FDADecember 2, 2017device

Volumat MC Agilia Volumetric Infusion Pump, Model No. Z021135, Software version 1.7. Product Usage - The Volumat MC Agilia is a piece of transportable medical equipment intended to be used in healthcare facilities environment by healthcare trained professionals according to hospital protocols on ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

fresenius vial safreseniusfresenius vial

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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