Novum IQ LVP
Brand(s)
Last updated
Summary
Product
Novum IQ LVP
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue |
|---|---|---|
| Novum IQ LVP | All lots. | 40700BAX |
Issue
Baxter is issuing an urgent medical device correction for the Novum IQ Large Volume Pump (LVP) due to the following two issues:
- there is a potential for underinfusion when transitioning from a lower to a higher flow rate (e.g., rate change or bolus). Specifically, the risk occurs when the second flow rate is more than double the first flow rate.
- Baxter has identified an increase in customer reports of over and underinfusion that may be due to set misloading. Failure to properly load the tubing into the pump channel may result in the pump infusing at a rate higher or lower than programmed.
Recall start date: July 17, 2025
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies
| Baxter Healthcare Corporation |
| 1 Baxter Parkway, Deerfield, Illinois, United States, 60015 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-77756
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