FDA Device recall Z-2333-2025
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
- FDA Device
- Class I
- ongoing
- Published 2025-09-10
On 2025-09-10 the FDA classified a Class I recall of Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump by Baxter Healthcare, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2333-2025 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2025-08-04 |
| Published | 2025-09-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | PR |
Product
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
Reason
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).
Identifiers
| code_info | UDI/DI 05413765852428, All Serial Numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2333-2025%22
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