Baxter Novum IQ LVP INFUSION SYSTEM — Class I medical device recall Z-1767-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2025-05-28. There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby
| Recall number | Z-1767-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-04-24 |
| Classified | 2025-05-20 |
| Reported by FDA | 2025-05-28 |
| Countries outside the US | CA |
| Quantity | 34,524 units |
| Model numbers | 40700BAXUS |
Product
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Reason for recall
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.
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-1767-2025. 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.