Recall archive / FDA device enforcement
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS — FDA record Z-1767-2025
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 Apr 24, 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
- Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
- Reason
- There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.
- Classification
- Class I
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 34,524 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1767-2025
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 | All serial numbers |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US and Canada
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- May 28, 2025
- Recall initiation date
- Apr 24, 2025
- Center classification date
- May 20, 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.