Baxter Novum IQ LVP Infusion System recall
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Why was Baxter Novum IQ LVP Infusion System recalled?
There is a potential for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature or if the device is powered off with the set loaded.
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?
All serial numbers
- Product
- Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 34,524 units
- Distribution
- US and Canada
- Recall date
- May 28, 2025
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)