Viatris recalls
12 official recalls and safety alerts involving Viatris since 2021-10, from FDA · Drug. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Viatris or the relevant agency.
- 2026-04-15
US- 2025-01-22
- US
Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8 mg, 30-count bottle, Rx only, Distributed by Viatris Specialty LLC, Morgantown, WV…
Failed Impurities/Degradation Specifications: Out of specification results observed for the impurity compound B during stability testing.
- 2024-12-18
- US
Viatris Inc recalls Levothyroxine Sodium Tablets USP, 150 mcg, packaged in a) 90-count bottles (NDC 0378-1815-77) and b) 1000-count bottles (NDC…
Superpotent Drug and Subpotent Drug: potency failures obtained
- 2024-07-24
- US
Viatris Inc recalls Cardura XL (doxazosin) extended release tablets 8mg, 30-count bottles, Rx Only Made in Singapore, Distributed by Roerig Division of Pfizer…
Failed Impurities/Degradation Specifications
- 2024-05-08
- US
Viatris Inc recalls Valacyclovir Tablets USP, 500 mg, 90 count bottles, Rx Only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC…
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
- 2023-06-14
- US
Viatris Inc recalls Levsin injection (hyoscyamine sulfate injection, USP), 0.5 mg per ml in water for Injection, 1 ml Ampule (Box of 5 ampules), Rx Only,…
CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
FDA · DrugViatris IncProduct was distributed to 10 distributors who may have further distribute the…Official notice → - 2022-11-23
- US
Viatris Inc recalls Carvedilol Tablets, USP, 25 mg, 500-count bottles, Rx Only, Mfg: Mylan Pharmaceuticals Inc. Morgantown, WV 36505, Made in India, NDC…
Failed Tablet/Capsule Specifications: Tablets exceeds specification for weight and thickness.
- 2022-11-16
- US
Viatris Inc recalls Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only,…
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
- 2022-10-05
- US
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, Rx only, Mylan…
Presence of Particulate Matter: A complaint was received for the presence of a single strand of hair in one vial.
- 2022-05-18
- US
Viatris Inc recalls Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer…
Failed Dissolution Specifications: low out of specification results for dissolution.
- 2022-05-11
- US
Viatris Inc recalls alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
- 2021-10-06
- US