Viatris recalls 90-count and 1000-count Levothyroxine Sodium Tablets (112 mcg) due to potency failures. Affected lots expire Feb 2025 or later. Contact for return instructions.
Superpotent Drug and Subpotent Drug: potency failures obtained
Viatris is recalling Levothyroxine Sodium Tablets (112 mcg) in 90-count and 1000-count bottles because they may have potency failures. This means the medication might not work as intended, potentially causing health issues if taken without proper dosage.
Potency failures mean the medication may not contain the correct amount of active ingredient. This could lead to improper treatment of thyroid conditions if taken without the right dosage.
People prescribed levothyroxine who own the recalled bottles (NDC 0378-1811-77 or 0378-1811-10) are affected. Those with thyroid conditions are most at risk.
Check for 90-count or 1000-count bottles labeled 'Levothyroxine Sodium Tablets USP, 112 mcg'. The NDC codes are 0378-1811-77 or 0378-1811-10. The expiration dates range from February 2025 to November 2024.
Identify the NDC code on the bottle (0378-1811-77 or 0378-1811-10) and expiration date.
The medication may have potency failures, meaning it might not contain the correct amount of active ingredient.
The recall record does not specify a remedy, so contact Viatris directly for instructions.
Potency failures could lead to improper treatment of thyroid conditions if taken without the right dosage, but the recall indicates low risk.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0128-2025 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0128-2025 from Viatris. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.