Day

August 29, 2025
29
Aug

FDA Recall: Software anomalies that may result in a blank Run screen

August 29, 2025
Company: Baxter Healthcare Corporation Date of Enforcement Report: 8/29/2025 Class: I PRODUCT Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump Recall Number: Z-2332-2025 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...
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