Z-1767-2025 Class I Ongoing
FDA device recall Z-1767-2025 was initiated by Baxter Healthcare Corporation on April 24, 2025 and is designated Class I. Reason for recall: 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. The recall status is ongoing. Affected quantity: 34,524 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 28, 2025
- Initiation Date
- April 24, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 34,524 units
Product Description
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Reason for Recall
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.
Distribution Pattern
US and Canada
Code Information
All serial numbers