Viatris Inc 2024-12-18 Health serious FDA
Health · FDA · Recall #FDA-D-0127-2025
Levothyroxine Sodium Tablets USP, 100 mcg, packaged in a) 90-count bottles (NDC… Recall
Issued December 18, 2024 · Viatris Inc
In December 2024, Viatris Inc recalled the Levothyroxine Sodium Tablets USP, 100 mcg, packaged in a) 90-count bottles (NDC…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Superpotent Drug and Subpotent Drug: potency failures obtained
What you should do
- 1 Stop using Levothyroxine Sodium Tablets USP, 100 mcg, packaged in a) 90-count bottles (NDC… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Viatris Inc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Viatris Inc
- Category
- Health
- Recall date
- December 18, 2024
- Units affected
- Not reported
- Sold at
- Nationwide within the United States and Puerto Rico
- Recall number
- FDA-D-0127-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- Viatris Inc has 9 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.