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 high severity by Argus HQ. FDA published the underlying record on 2025-06-18; 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 · high

Baxter Healthcare Corporation — Class II recall: Baxter Novum IQ Syringe Pump, product code 40800BAXUS,

Name: FDA Recall Record — Baxter Healthcare Corporation
Creator: Argus HQ
Published: 2025-06-18
License: https://argushq.ai/methodology

Event date: 2025-06-18 00:00:00Z
Observed: 2026-07-16 23:20:09Z
Source ID: Z-1964-2025
Payload hash: bcbfb120958967f6838b79d4…

Summary

Baxter has identified a design issue which may cause the pump to detect the presence of a syringe flange when no syringe is loaded. When this issue occurs, the pumps 'user interface becomes stuck on the "Remove Syringe" screen when an infusion is complete, and the syringe is unloaded. A System Error… 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 high severity by Argus HQ. FDA published the underlying record on 2025-06-18; 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 II recall: Baxter Novum IQ Syringe Pump, product code 40800BAXUS,. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1964-2025

MLA

"Baxter Healthcare Corporation — Class II recall: Baxter Novum IQ Syringe Pump, product code 40800BAXUS,." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1964-2025.

Chicago

Argus HQ Research. "Baxter Healthcare Corporation — Class II recall: Baxter Novum IQ Syringe Pump, product code 40800BAXUS,." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1964-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_baxter_healthcare_corporation_z_1964_2025_2025,
  title = {Baxter Healthcare Corporation — Class II recall: Baxter Novum IQ Syringe Pump, product code 40800BAXUS,},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1964-2025},
  note = {Accessed: July 23, 2026}
}

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