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FDAAugust 11, 2026

Baxter Novum IQ Syringe Pump Recall Over Software Issue in Multi-Syringe Infusion (Aug 11, 2026)

FDA published this notice on August 11, 2026 for United States.

This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.

What AreaZine recorded

Agency
FDA
Place
United States
Date
August 11, 2026
Recall class
Class II
Reason given by the agency
A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused (VTBI) remains.
Distribution
US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV.
Official source
the notice at its source

Official warnings by state, with every type counted since 2008Search notices, places and declaration numbers

Source: FDA.

The record around this notice