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 2024-07-17; 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: Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150…

Name: FDA Recall Record — Baxter Healthcare Corporation
Creator: Argus HQ
Published: 2024-07-17
License: https://argushq.ai/methodology

Event date: 2024-07-17 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-2323-2024
Payload hash: f82be20f5c1dff60c0a7a735…

Summary

During manufacturing, the step to install an Electromagnetic Interference (EMI) Absorber was omitted. The purpose of the EMI absorber is to prevent EMI leakage that might potentially affect other devices in the vicinity or the device itself may be vulnerable to EMI resulting in device malfunction or… 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 2024-07-17; 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: Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2323-2024

MLA

"Baxter Healthcare Corporation — Class II recall: Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150…." Argus HQ Research, Digital Empire LLC, 2024, argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2323-2024.

Chicago

Argus HQ Research. "Baxter Healthcare Corporation — Class II recall: Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2323-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_baxter_healthcare_corporation_z_2323_2024_2024,
  title = {Baxter Healthcare Corporation — Class II recall: Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2323-2024},
  note = {Accessed: July 17, 2026}
}

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