Recall Atlas
Drugs & medicalClass III

Viatris, Inc. recalls Telmisartan and Amlodipine, Tablets, USP, 40mg/5 mg, 30-count Bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown,…

Superpotent Drug: potential for the Telmisartan content in these lots to exceed specifications

Read the official notice →
Date
2026-10-28
Country
United States
Brand
Viatris
Product
Telmisartan and Amlodipine, Tablets, USP, 40mg/5 mg, 30-count Bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown,…
Classification
Class III
Units
Nationwide in the USA.
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Viatris recalls

  1. 2026-04-15
  2. 2025-01-22
  3. Drugs & medicalClass II

    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.

    FDA · DrugViatris IncUSA nationwide.Official notice →
  4. 2024-12-18
  5. Drugs & medicalClass II

    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

    FDA · DrugViatris IncNationwide within the United States and Puerto RicoOfficial notice →
  6. 2024-07-24
  7. 2024-05-08
  8. Drugs & medicalClass III

    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.

    FDA · DrugViatris IncNationwide within the united statesOfficial notice →
  9. 2023-06-14
  10. Drugs & medicalClass II

    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 →
All 13 Viatris recalls →

Other drugs & medical recalls in the United States

  1. 2026-10-28
  2. Drugs & medicalClass II

    Pfizer recalls Levoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 100 tablet bottle, Rx only, Distributed by Pfizer Inc., New York, NY 10017,…

    Subpotent Drug: confirmed out-of-specification (OOS) assay during stability testing.

    FDA · DrugPfizerUS Nationwide and Puerto RicoOfficial notice →
  3. Drugs & medicalClass II

    Shenzhen Techdow Pharmaceutical Co., Ltd. recalls Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1mL Multi dose vial x 25 vials per carton, Distributed by: Hepalink…

    Lack of Assurance of Sterility

    FDA · DrugShenzhen Techdow Pharmaceutical Co., Ltd.Nationwide in the USA.Official notice →
  4. Drugs & medicalClass II

    Ascend Laboratories, LLC recalls Amlodipine and Olmesartan Medoxomil Tablets, 10mg/40mg, 30 Tablets, Rx only, Manufactured by: Alkem Laboratories Ltd., INDIA,…

    Out of specification due to dissolution.

    FDA · DrugAscend Laboratories, LLCNationwide within the United StatesOfficial notice →
  5. 2026-10-21
  6. Drugs & medicalClass II

    Radiometer Medical ApS recalls The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and therapists. It is…

    In vitro diagnostic analyzer had a risk of potentially inaccurate results requiring changes to instructions for use and: 1) Sample types, including whole blood samples no longer suitable for testing FHbF and ctBil, 2)…

    FDA · DeviceRadiometer Medical ApSUS Nationwide distribution including in the states of CA, OH, LA, MA, FL, NY,…Official notice →
See all drugs & medical recalls →