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 critical severity by Argus HQ. FDA published the underlying record on 2026-08-19; Argus observed and indexed it on 2026-08-26.

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: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; So…

Name: FDA Recall Record — Baxter Healthcare Corporation
Creator: Argus HQ
Published: 2026-08-19
License: https://argushq.ai/methodology

Event date: 2026-08-19 00:00:00Z
Observed: 2026-08-26 04:20:38Z
Source ID: Z-2766-2026
Payload hash: e3625b36e96552039b905588…

Summary

Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open position. 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 critical severity by Argus HQ. FDA published the underlying record on 2026-08-19; Argus observed and indexed it on 2026-08-26.
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 (2026). Baxter Healthcare Corporation — Class I recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; So…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2766-2026

MLA

"Baxter Healthcare Corporation — Class I recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; So…." Argus HQ Research, Digital Empire Holdings LLC, 2026, argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2766-2026.

Chicago

Argus HQ Research. "Baxter Healthcare Corporation — Class I recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; So…." Digital Empire Holdings LLC. Accessed August 27, 2026. https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2766-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_baxter_healthcare_corporation_z_2766_2026_2026,
  title = {Baxter Healthcare Corporation — Class I recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; So…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-2766-2026},
  note = {Accessed: August 27, 2026}
}

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