Recall archive / FDA device enforcement
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump — FDA record Z-2333-2025
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 4, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
- Reason
- 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).
- Classification
- Class I
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 10,101 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2333-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 05413765852428, All Serial Numbers |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US distribution including Puerto Rico and OUS (International) Canada
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Sep 10, 2025
- Recall initiation date
- Aug 4, 2025
- Center classification date
- Aug 29, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.