FDAFDA · Food and drugs·Recall number Z-2333-2025
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
Published September 10, 2025 · Recall initiated: August 4, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's 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
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- US distribution including Puerto Rico and OUS (International) Canada
- Lot
- UDI/DI 05413765852428, All Serial Numbers
- Risk classification
- Class I
- Area (FDA)
- device
- Country
- United States
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