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Baxter Healthcare Corporation recalls Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump
Recalled September 10, 2025 · FDA recall Z-2334-2025 · Baxter Healthcare
Hazard
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). · FDA Class I
Units
22703 units
Sold at
US distribution including Puerto Rico and OUS (International) Canada
Description
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).
Product
Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →