Reported Apr 2, 2025 · Ongoing

Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Lot codes and dates
  • UDI/DI 05413765852428
  • Serial Numbers

    149 of 149 codes

    • 02A220600103
    • 02A221100387
    • 02A240800201
    • 02A230300471
    • 02A240800161
    • 02A220600112
    • 02A230100474
    • 02A240800343
    • 02A230400357
    • 02A240800175
    • 02A220700259
    • 02A230200471
    • 02A240800710
    • 02A230600165
    • 02A240800223
    • 02A220700176
    • 02A230200487
    • 02A240900081
    • 02A230600175
    • 02A240800513
    • 02A220700349
    • 02A230300030
    • 02A240900133
    • 02A230600176
    • 02A240800577
    • 02A220700268
    • 02A230300117
    • 02A240900265
    • 02A230600255
    • 02A240900261
    • 02A220700081
    • 02A230300125
    • 02A240900277
    • 02A230600256
    • 02A240900421
    • 02A220700140
    • 02A230300132
    • 02A240900285
    • 02A230600618
    • 02A240900742
    • 02A220700351
    • 02A230300146
    • 02A240900287
    • 02A230700137
    • 02A240900746
    • 02A220700409
    • 02A230300275
    • 02A240900282
    • 02A241000576
    • 02A240901067
    • 02A220700368
    • 02A230300287
    • 02A240900373
    • 02A220700166
    • 02A240901181
    • 02A220700428
    • 02A230300309
    • 02A240900407
    • 02A221000108
    • 02A240901422
Amount recalled
149 units

This recall covers 16 products

The agency filed one notice per product. You are reading one of them; the other 15 are below.

3 more are in the archive.

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:43 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.