Novum IQ Syringe Pump — Class I medical device recall Z-2334-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2025-09-10, distributed in PR. Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pum
| Recall number | Z-2334-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-08-04 |
| Classified | 2025-08-29 |
| Reported by FDA | 2025-09-10 |
| Distributed | PR |
| Countries outside the US | CA |
| Quantity | 22,703 units |
| Reason classes | software |
Product
Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump
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 blank Run screen (LVP and SP) and/or false motor movement system error (SP only).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2334-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.