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 medium severity by Argus HQ. FDA published the underlying record on 2024-05-08; 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 · medium

Viatris Inc — Class III recall: Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: M…

Name: FDA Recall Record — Viatris, Inc.
Creator: Argus HQ
Published: 2024-05-08
License: https://argushq.ai/methodology

Event date: 2024-05-08 00:00:00Z
Observed: 2026-07-16 23:20:07Z
Source ID: D-0481-2024
Payload hash: 98058787aea2865a495d0b40…

Summary

Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets. Status: Completed.

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 medium severity by Argus HQ. FDA published the underlying record on 2024-05-08; 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). Viatris Inc — Class III recall: Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: M…. Digital Empire Holdings LLC. Retrieved from https://argushq.ai/events/fda-recall-viatris-inc-d-0481-2024

MLA

"Viatris Inc — Class III recall: Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: M…." Argus HQ Research, Digital Empire Holdings LLC, 2024, argushq.ai/events/fda-recall-viatris-inc-d-0481-2024.

Chicago

Argus HQ Research. "Viatris Inc — Class III recall: Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: M…." Digital Empire Holdings LLC. Accessed July 23, 2026. https://argushq.ai/events/fda-recall-viatris-inc-d-0481-2024.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_viatris_inc_d_0481_2024_2024,
  title = {Viatris Inc — Class III recall: Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: M…},
  author = {{Argus HQ Research}},
  year = {2024},
  publisher = {Digital Empire Holdings LLC},
  url = {https://argushq.ai/events/fda-recall-viatris-inc-d-0481-2024},
  note = {Accessed: July 23, 2026}
}

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