Official recall record
Novum IQ LVP (ref 77756)
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-07-22
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.