Has Viatris, Inc. had other FDA enforcement actions?

Yes. Argus HQ has recorded 18 total FDA actions tied to Viatris, Inc.: 0 warning letters, 18 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 2025-01-22; 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 · drug_recall · high

Viatris Inc — Class II recall: Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only,…

Name: FDA Recall Record — Viatris, Inc.
Creator: Argus HQ
Published: 2025-01-22
License: https://argushq.ai/methodology

Event date: 2025-01-22 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: D-0203-2025
Payload hash: 5e42cbe602f74a7780e3f6f0…

Summary

Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing. Status: Terminated.

Entities

Viatris, Inc.

View source record ↗

Frequently asked questions

Has Viatris, Inc. had other FDA enforcement actions?: Yes. Argus HQ has recorded 18 total FDA actions tied to Viatris, Inc.: 0 warning letters, 18 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 2025-01-22; 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). Viatris Inc — Class II recall: Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only,…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-viatris-inc-d-0203-2025

MLA

"Viatris Inc — Class II recall: Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only,…." Argus HQ Research, Digital Empire Holdings LLC, 2025, argushq.ai/events/fda-recall-viatris-inc-d-0203-2025.

Chicago

Argus HQ Research. "Viatris Inc — Class II recall: Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only,…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-viatris-inc-d-0203-2025.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_viatris_inc_d_0203_2025_2025,
  title = {Viatris Inc — Class II recall: Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only,…},
  author = {{Argus HQ Research}},
  year = {2025},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-viatris-inc-d-0203-2025},
  note = {Accessed: July 23, 2026}
}

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