Official recall record
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2025-08-04
- Country of alert
- United States
- Alert level
- Class I
- Alert type
- recall
- Barcode (EAN/GTIN)
- 05413765852428
- Brand on record
- Baxter Healthcare Corporation
What the authority reported
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).
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 2 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2025-05-12 · US FDA — Medical Devices
Baxter Novum IQ Syringe Pump, product code 40800BAXUS, - 2026-08-11 · US FDA — Medical Devices
Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
Other recalls from this brand
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All 43 official recall notices naming Baxter Healthcare Corporation on this site →