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Home › FDA recalls › Levothyroxine Sodium Tablets
CLASS II · ModerateFDA

Major Pharmaceuticals recalls Levothyroxine Sodium Tablets

📅 Jul 13, 2026 · 📍 Nationwide
Recalling company
Major Pharmaceuticals
Product
Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg), 10 Tablets (10 x 1) unit dose blisters per carton, Rx only, Packaged and Distributed by: MAJOR PHARMACEUTICALS, Indianapolis, IN 46268 USA. Distributed by Cardinal Health, Dublin, OH 43017. NDC Bag: 55154-3559-0; NDC Blister: 0904-6950-61
Reason
Subpotent Drug
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Jul 13, 2026
Reported
Jul 29, 2026
Distribution
Nationwide in the USA.
Status
Ongoing
Quantity
N/A
Lot / codes
Bag lot #: N02200A, N02200B, Exp. Date 10/2026; Blister lot #: N02200, Exp. Date 10/2026
Company location
Dublin, OH
Recall type
Voluntary: Firm initiated
Recall number
D-0708-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0708-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.