Viatris recalls Levothyroxine Sodium Tablets (88 mcg) with potency failures. These tablets may not provide correct hormone levels, risking health issues. Check NDC codes and expiration dates for affected batches.
Superpotent Drug and Subpotent Drug: potency failures obtained
Viatris is recalling Levothyroxine Sodium Tablets (88 mcg) due to potency failures. This means the medication may not work correctly, potentially causing health problems if taken without proper dosage.
Potency failures mean the medication may not contain the correct amount of active ingredient. This could lead to incorrect hormone levels, affecting thyroid function and potentially causing health issues.
People prescribed levothyroxine who own the recalled 90-count or 1000-count bottles with specific NDC numbers and expiration dates. Those with thyroid conditions are most at risk.
Check for NDC codes 0378-1807-77 (90-count bottles) or 0378-1807-10 (1000-count bottles). Also look for expiration dates listed in the recall: August 2025, February 2025, April 2025, January 2025, December 2024, or August 2025.
Identify the NDC code and expiration date on your bottle to confirm if it's in the recalled batches.
The recall states there are potency failures, so the tablets may not provide the correct hormone levels. Do not take these tablets without consulting a healthcare provider.
The recall does not specify a remedy, so contact your healthcare provider for guidance on safe alternatives.
Check for NDC codes 0378-1807-77 (90-count) or 0378-1807-10 (1000-count) and expiration dates listed in the recall.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0126-2025 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0126-2025 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.
