Drug recall
Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump
FDA recall event 97296 · Class I · Baxter Healthcare Corporation
Key facts
| Event ID | 97296 |
|---|---|
| Recall numbers | Z-2332-2025, Z-2333-2025, Z-2334-2025 |
| Recalling firm | Baxter Healthcare Corporation |
| Product type | Devices |
| Products | Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump, Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump, Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Aug 4, 2025 |
| Report date | Sep 10, 2025 |
| City | Deerfield |
| State | IL |
| Country | United States |
| FEI number | 1417572 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: