FDAAugust 4, 2025device
Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
What to do
FDA enforcement status: Ongoing
Brands named
baxter healthcarebaxter
UPCs
05413765851797
Recall history
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