Baxter NovumIQ Syringe INFUSION SYSTEM — Class II medical device recall Z-1423-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2025-04-02, distributed nationwide. Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed
| Recall number | Z-1423-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-03-03 |
| Classified | 2025-03-21 |
| Reported by FDA | 2025-04-02 |
| Distributed | Nationwide (US) |
| Quantity | 149 units |
| UPC / GTIN / UDI-DI | 05413765852428 |
| Serial numbers | 02A220600103, 02A220600112, 02A220700081, 02A220700140, 02A220700166, 02A220700176, 02A220700259, 02A220700268, 02A220700349, 02A220700351, 02A220700368, 02A220700409, 02A220700428, 02A220700450, 02A220700454, 02A220700458, 02A220800010, 02A220800060, 02A220800201, 02A220800407, 02A221000099, 02A221000108, 02A221000109, 02A221000233, 02A221000240 and 124 more |
| Model numbers | 40800BAXUS |
Product
Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Reason for recall
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.
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-1423-2025. 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.