FDA recall Z-1767-2025

Product

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

US and Canada

Key facts

Status

Ongoing

Initiation date

2025-04-24

Report date

2025-05-28

Voluntary/Mandated

Voluntary: Firm initiated

Location

Deerfield, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1767-2025