FDA Medical devices recall ·
Baxter Novum IQ LVP INFUSION SYSTEM recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-1767-2025
- Date
- (initiated April 24, 2025)
- Company / brand
- Baxter Healthcare Corporation
1 Baxter Pkwy, Deerfield, IL, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 34,524 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Why was it 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 you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All serial numbers
Distribution
US and Canada
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-1767-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.