Major Pharmaceuticals Levothyroxine Recall
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 Tablets (10 x 10 unit dose blisters) per carton, Rx only, Packaged and Distributed
Updated July 13, 2026
Major Pharmaceuticals is recalling Levothyroxine Sodium 88 mcg tablets because they are subpotent, meaning they contain less active ingredient than labeled. This puts patients at risk of insufficient thyroid hormone replacement.
Is the Major Pharmaceuticals recalled? Yes. This product was recalled by FDA on July 13, 2026. Details below.
What is recalled
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 100 tablets per carton (10 x 10 unit dose blisters), Rx only, packaged and distributed by Major Pharmaceuticals, Indianapolis, IN 46268. NDC: 0904-6952-61.
Am I affected
You're affected if your prescription bottle shows the NDC number 0904-6952-61 and the strength is 88 mcg levothyroxine sodium tablets.
What to do right now
Contact your pharmacy or Major Pharmaceuticals immediately to return or replace this medication. Do not stop taking your levothyroxine without consulting your doctor, as this could affect your thyroid condition. Ask your doctor or pharmacist for guidance on obtaining a replacement supply.
The hazard
Subpotent Drug
Brands affected
- Source
- FDA
- Category
- Drugs & Medications
- Recall ID
- fda-D-0703-2026
- Classification
- Class II
- Recalled
- July 13, 2026
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