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FDA · FDA event 97296 · Posted Aug 29, 2025
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).
The official notice takes precedence over this summary. Talk to your clinician before changing prescribed therapy.
| Model | Description | Lot / serial range | Manufactured | Status |
|---|---|---|---|---|
| Z-2334-2025 | Z-2334-2025 | UDI/DI N/A, All Serial Numbers | Not provided in the normalized record | Ongoing |
| Z-2333-2025 | Z-2333-2025 | UDI/DI 05413765852428, All Serial Numbers | Not provided in the normalized record | Ongoing |
| Z-2332-2025 | Z-2332-2025 | UDI/DI 05413765851797, All Serial Numbers | Not provided in the normalized record | Ongoing |
Aug 4, 2025
Recall initiated
Date recorded by the FDA.
Aug 29, 2025
Posted by FDA
The recall event appeared in the FDA source.
Oct 8, 2026
Last checked
MedWatcher last reconciled this record with the openFDA export.