Viatris recalls
Every recall we track for Viatris — 2 in all, all from 2021 — plus the complaints and injury reports the public filed about them. 1 is rated “stop using now”.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Viatris since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 1 | 0 | 0 | 1 | 2 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Viatris product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Viatris recalls
2 shown- Stop using nowDrug
Viatris recalls Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown,
Viatris recalls 16mg Candesart: Impurities may cause serious harm. Affected lots from October 2021. Stop using and contact for replacement.
ViatrisSep 13, 2021 - UnratedDrug
Viatris recalls Lyrica CR (pregabalin) extended release tablets, 330 mg, 30-count bottles, Rx only, Distributed by Parke-Davis Division
Viatris recalls 330mg Lyrica CR extended-release tablets with failed dissolution specifications. Rx-only bottles distributed by Parke-Davis Division of Pfizer. No remedy specified in official notice.
ViatrisAug 23, 2021
Viatris recall questions
How many recalls has Viatris had?
2 recalls from Viatris are on record with U.S. safety agencies, from 2021.
What is the most recent Viatris recall?
Viatris recalls Candesartan Cilexetil Tablets, USP 16 mg, 30 count bottles, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown,, dated Sep 13, 2021. Every Viatris recall is listed on this page, newest first.
What should I do if I have a recalled Viatris product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Viatris recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.