Baxter Novum IQ Syringe Pump recall
Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
Why was Baxter Novum IQ Syringe Pump recalled?
Baxter has identified a design issue which may cause the pump to detect the presence of a syringe flange when no syringe is loaded. When this issue occurs, the pumps 'user interface becomes stuck on the "Remove Syringe" screen when an infusion is complete, and the syringe is unloaded. A System Error 21502 (Flange Sensor Failure) may occur. Please note this issue only affects a subset of Novum IQ syringe pumps manufactured or repaired after July 4, 2023.
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
- Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 8027 units
- Distribution
- US Nationwide distribution.
- Recall date
- June 18, 2025
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)