Viatris recalls 90-count and 1000-count Levothyroxine Sodium Tablets USP 175 mcg due to potency failures. These tablets may not provide correct thyroid hormone levels, risking health issues.
Superpotent Drug and Subpotent Drug: potency failures obtained
Viatris is recalling Levothyroxine Sodium Tablets USP 175 mcg in 90-count and 1000-count bottles because they may have potency failures. This means the medication might not work correctly, leading to improper thyroid hormone levels and potential health risks.
Potency failures mean the tablets may not contain the correct amount of active drug. This can lead to incorrect thyroid hormone levels, which might cause health issues like fatigue, weight changes, or other thyroid-related problems.
People who have been prescribed Levothyroxine Sodium Tablets USP 175 mcg by a doctor. Those with thyroid conditions are most at risk if the medication isn't working properly.
Check for 90-count bottles (NDC 0378-1817-77) or 1000-count bottles (NDC 0378-1817-10) with lot numbers 3192915, 8172108 (expiring March 2025) or 3208680 (expiring September 2025).
Look for the product's NDC codes and lot numbers to confirm if it's part of the recall.
The recall is due to potency failures, meaning the tablets may not contain the correct amount of active drug, which could lead to improper thyroid hormone levels.
Check the product details to see if it's part of the recall. If it is, contact your doctor for alternative medication options.
Yes, avoid lot numbers 3192915, 8172108 (expiring March 2025) for 90-count bottles and lot number 3208680 (expiring September 2025) for 1000-count bottles.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0121-2025 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0121-2025 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.
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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.
