Viatris recalls

Viatris has 25 recalls on record with the FDA and USDA, the earliest in 2021 and the latest reported on 15 Apr 2026. 12 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is potency & assay.

Total recalls25since 2021
Last 12 months1reported
Class I14% of total
Ongoing12latest 15 Apr 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 4%Class II 22 88%Class III 2 8%

By year

Ongoing viatris recalls

12 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIXanax XR, alprazolam, extended-release tablets, 3 mg recalled by ViatrisXanaxViatrisPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets USP, 25 mcg recalled by ViatrisLevothyroxine SodiumViatrisPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets USP, 75 mcg recalled by ViatrisLevothyroxine SodiumViatrisPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets USP, 88 mcg recalled by ViatrisLevothyroxine SodiumViatrisPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets USP, 137 mcg recalled by ViatrisLevothyroxine SodiumViatrisPotency & AssayNationwide
DrugCLASS IILevothyroxine Sodium Tablets USP, 175 mcg recalled by ViatrisLevothyroxine SodiumViatrisPotency & AssayNationwide

All viatris recalls, newest first

25 total

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.