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Baxter Healthcare Corporation recalls Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Recalled May 28, 2025 · FDA recall Z-1767-2025 · Baxter Healthcare
Hazard
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. · FDA Class I
Units
34,524 units
Sold at
US and Canada
Description
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.
Product
Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →