Has Baxter Healthcare Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 208 total FDA actions tied to Baxter Healthcare Corporation: 0 warning letters, 208 recalls, 0 approval records, and 0 Form 483 inspection citations.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2025-09-10; Argus observed and indexed it on 2026-07-16.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · critical

Baxter Healthcare Corporation — Class I recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

Name: FDA Recall Record — Baxter Healthcare Corporation
Creator: Argus HQ
Published: 2025-09-10
License: https://argushq.ai/methodology

Event date: 2025-09-10 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-2333-2025
Payload hash: 297c1516061ed8f4e8ceac1a…

Summary

Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only). Status: Ongoing.

Entities

Baxter Healthcare Corporation

View source record ↗

Frequently asked questions

Has Baxter Healthcare Corporation had other FDA enforcement actions?: Yes. Argus HQ has recorded 208 total FDA actions tied to Baxter Healthcare Corporation: 0 warning letters, 208 recalls, 0 approval records, and 0 Form 483 inspection citations.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged critical severity by Argus HQ. FDA published the underlying record on 2025-09-10; Argus observed and indexed it on 2026-07-16.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2025). Baxter Healthcare Corporation — Class I recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2333-2025

MLA

"Baxter Healthcare Corporation — Class I recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump." Argus HQ Research, Digital Empire LLC, 2025, argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2333-2025.

Chicago

Argus HQ Research. "Baxter Healthcare Corporation — Class I recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2333-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_baxter_healthcare_corporation_z_2333_2025_2025,
  title = {Baxter Healthcare Corporation — Class I recall: Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2333-2025},
  note = {Accessed: July 17, 2026}
}

Informational only. Not legal, financial, or medical advice.