FDAMarch 3, 2025device

Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

05413765852428

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS — Recall Details · AllClear