Has Baxter Healthcare Corporation had other FDA enforcement actions?

Yes. Argus HQ has recorded 209 total FDA actions tied to Baxter Healthcare Corporation: 0 warning letters, 209 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 2024-08-28; 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 Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with…

Name: FDA Recall Record — Baxter Healthcare Corporation
Creator: Argus HQ
Published: 2024-08-28
License: https://argushq.ai/methodology

Event date: 2024-08-28 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-2581-2024
Payload hash: 798836a57bfe9e857911b22e…

Summary

The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system. 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 209 total FDA actions tied to Baxter Healthcare Corporation: 0 warning letters, 209 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 2024-08-28; 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 (2024). Baxter Healthcare Corporation — Class II recall: Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2581-2024

MLA

"Baxter Healthcare Corporation — Class II recall: Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with…." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2581-2024.

Chicago

Argus HQ Research. "Baxter Healthcare Corporation — Class II recall: Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with…." Digital Empire Holdings LLC. Accessed August 31, 2026. https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2581-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_baxter_healthcare_corporation_z_2581_2024_2024,
  title = {Baxter Healthcare Corporation — Class II recall: Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2581-2024},
  note = {Accessed: August 31, 2026}
}

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