Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Levothyroxine Sodium Tablets USP Recalled by Viatris Inc Due to Superpotent Drug and Subpotent Drug: potency failures obtained
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Viatris Inc directly.
Affected Products
Levothyroxine Sodium Tablets USP, 88 mcg, packaged in a) 90-count bottles (NDC 0378-1807-77) and b) 1000-count bottles (NDC 0378-1807-10), Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A.
Quantity: 43,765 bottles
Why Was This Recalled?
Superpotent Drug and Subpotent Drug: potency failures obtained
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viatris Inc
Viatris Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report