Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2333-2025 — Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

U.S. FDA — Device Enforcement · United States · 2025-08-04 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2333-2025
Date of alert
2025-08-04
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Baxter Healthcare Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05413765852428
Reported risk: 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).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.