Viatris, Inc. recalls
Every recall we track for Viatris, Inc. — 23 in all, from 2022–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Viatris, Inc. dropped to zero in 2025 (0, down from 16 in 2024).
All FDA recall records for Viatris, Inc. 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 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 2 | 3 | 0 | 5 |
| 2023 | 0 | 0 | 0 | 1 | 1 |
| 2024 | 0 | 0 | 13 | 3 | 16 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
Most common reasons for Viatris, Inc. recalls
What to do if you have a recalled Viatris, Inc. 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, Inc. recalls
11 shown- Lower riskDrug
Viatris, Inc. recalls Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty
Viatris recalls 3mg Xanax XR tablets with failed dissolution specs. This may affect medication effectiveness. Contact Viatris for details.
ViatrisMar 17, 2026 - Lower riskDrug
Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC,
Viatris recalls Cardura XL 8mg extended-release tablets due to impurity issues detected in stability testing. Affected lots may pose risks if stored improperly.
ViatrisDec 23, 2024 - Lower riskDrug
Viatris Inc recalls Levothyroxine Sodium Tablets USP, 150 mcg, packaged in a) 90-count bottles (NDC 0378-1815-77) and b) 1000-count bottles
Viatris recalls 150 mcg levothyroxine tablets with potency failures. Affected lots expire June 2025. Stop using if you have these specific NDC numbers.
ViatrisNov 18, 2024 - UnratedDrug
Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8mg, 30-count bottles, Rx Only Made in Singapore, Distributed by Roerig
Viatris recalls Cardura XL 8mg tablets made in Singapore with potential impurities. This recall affects specific lots of the prescription medication. Consumers should contact the manufacturer for details.
ViatrisApr 30, 2024 - Lower riskDrug
Viatris Inc recalls Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown,
Viatris recalls 500mg Valacyclovir tablets with possible missing 'M 122' imprint. This may affect identification and safety for prescription use.
ViatrisApr 25, 2024 - UnratedDrug
Viatris Inc recalls Levsin injection (hyoscyamine sulfate injection, USP), 0.5 mg per ml in water for Injection, 1 ml Ampule (Box of 5
Viatris recalls Levsin injection (0.5 mg/ml) due to quality program discontinuation. This may affect product identity, strength, quality, and purity. Check NDC #0037-9001-05 and lot 101241A.
ViatrisMay 25, 2023 - Lower riskDrug
Viatris Inc recalls Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made
Viatris recalls 25mg Carvedilol tablets due to weight and thickness exceeding specifications. This may affect medication accuracy. Check NDC 0378-3634-05 for affected lots.
ViatrisOct 21, 2022 - Use cautionDrug
Viatris Inc recalls Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous
Viatris recalls 10x1mL Octreotide syringes due to glass particles. Stop using if you have these syringes before expiration.
ViatrisOct 7, 2022 - Lower riskDrug
Viatris Inc recalls Ampicillin for Injection, USP, 2 grams/vial NDC 67457-352-02, packaged in 10 x 2 g vials per carton NDC 67457-352-10,
Viatris recalls Ampicillin injections due to a single strand of hair found in one vial. This may cause allergic reactions. Stop using affected lots immediately.
ViatrisSep 21, 2022 - Lower riskDrug
Viatris Inc recalls Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co,
Viatris recalls 3mg Xanax XR tablets with failed dissolution specs. This may affect medication effectiveness. Check NDC 0009-0068-07 and lot DX7983 for affected products.
ViatrisApr 28, 2022 - Use cautionDrug
Viatris Inc recalls alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ
Greenstone LLC recalls specific lots of 3 mg alprazolam XR tablets due to failed dissolution specifications. Check your bottle's lot number and expiration date.
GreenstoneApr 28, 2022
Viatris, Inc. recall questions
How many recalls has Viatris, Inc. had?
23 recalls from Viatris, Inc. are on record with U.S. safety agencies, from 2022–2026.
What is the most recent Viatris, Inc. recall?
Viatris, Inc. recalls Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty, dated Mar 17, 2026. Every Viatris, Inc. recall is listed on this page, newest first.
Why are Viatris, Inc. products recalled?
The most common reasons on record: Superpotent Drug and Subpotent Drug: potency failures obtained (11); Failed Impurities/Degradation Specifications (2).
What should I do if I have a recalled Viatris, Inc. 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, Inc. 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.