Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump
Reported: September 10, 2025 Initiated: August 4, 2025 #Z-2332-2025
Product Description
Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump
Reason for Recall
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).
Details
- Recalling Firm
- Baxter Healthcare Corporation
- Units Affected
- 43,922 units
- Distribution
- US distribution including Puerto Rico and OUS (International) Canada
- Location
- Deerfield, IL
Frequently Asked Questions
What product was recalled? ▼
Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump. Recalled by Baxter Healthcare Corporation. Units affected: 43,922 units.
Why was this product recalled? ▼
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).
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 10, 2025. Severity: Critical. Recall number: Z-2332-2025.
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