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 2023-03-15; 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 MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory…

Name: FDA Recall Record — Baxter Healthcare Corporation
Creator: Argus HQ
Published: 2023-03-15
License: https://argushq.ai/methodology

Event date: 2023-03-15 00:00:00Z
Observed: 2026-07-16 23:20:10Z
Source ID: Z-1213-2023
Payload hash: a2f018eb6eab3779ee31fe06…

Summary

MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches, which may have been incorrectly sealed, i.e., the pouches may have open or weak seals. This could lead to exposure to air, resulting in insufficient iodine/dry sponge inside the MiniCap, which could lead to the potential for i… 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 2023-03-15; 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 (2023). Baxter Healthcare Corporation — Class II recall: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1213-2023

MLA

"Baxter Healthcare Corporation — Class II recall: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory…." Argus HQ Research, Digital Empire LLC, 2023, argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1213-2023.

Chicago

Argus HQ Research. "Baxter Healthcare Corporation — Class II recall: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory…." Digital Empire LLC. Accessed July 17, 2026. https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1213-2023.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_baxter_healthcare_corporation_z_1213_2023_2023,
  title = {Baxter Healthcare Corporation — Class II recall: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution, 5C4466P; Accessory…},
  author = {{Argus HQ Research}},
  year = {2023},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-baxter-healthcare-corporation-z-1213-2023},
  note = {Accessed: July 17, 2026}
}

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