Baxter Healthcare Corporation Novum IQ Syringe infusion system, Product Code 40800BAXUS Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Novum IQ Syringe infusion system, Product Code 40800BAXUS
Brand
Baxter Healthcare Corporation
Lot Codes / Batch Numbers
All Serial Numbers
Products Sold
All Serial Numbers
Baxter Healthcare Corporation is recalling Novum IQ Syringe infusion system, Product Code 40800BAXUS due to Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Baxter is issuing an Urgent Medical Device Correction for the Novum IQ Syringe Pump. Baxter identified that after multiple downstream occlusion alarms, the pump may display an Infusion Complete alarm even though uninfused fluid remains in the syringe.
Recommended Action
Per FDA guidance
Baxter issued an "Urgent Medical Device Correction" notice on 10/13/2023 via USPS first-class mail. The notice explained the issue, hazard involved, and provided mitigation procedures in accordance with the Operator's Manual until a software upgrade becomes available. For additional questions or experience quality problems, please contact your Baxter sales representative, or Baxter Global Technical Services at 800-843-7867, Monday through Friday, between 7:00 am and 7:00 pm Eastern Time.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026