Novum IQ Syringe Pump recall: Software Issue
Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
Why was Novum IQ Syringe Pump 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).
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 05413765852428, All Serial Numbers
- Product
- Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 10,101 units
- Distribution
- US distribution including Puerto Rico and OUS (International) Canada
- Recall date
- September 10, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)