Recall
FDAHealthAugust 4, 2025

Baxter Healthcare Corporation — Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

⚠️ 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).

Is this relevant to me?

Geography
US
Source agency
FDA
Category
Health
Published
August 4, 2025

US distribution including Puerto Rico and OUS (International) Canada

What's affected?

Product
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
Lot code
UDI/DI 05413765852428, All Serial Numbers

Additional details

UDI/DI 05413765852428, All Serial Numbers

What should I do?

Recommended action

Class I recall. Voluntary: Firm initiated Quantity affected: 10,101 units.

View original FDA notice →

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