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

ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets

📅 Aug 6, 2026 · 📍 Nationwide
Recalling company
ACCORD HEALTHCARE, INC.
Product
Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), packaged in a) 90-count bottles (NDC 16729-451-15) and b) 1000-count bottles, (NDC 16729-451-17), Rx Only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: Intas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, India.
Reason
Subpotent Drug
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Aug 6, 2026
Reported
Sep 2, 2026
Distribution
Nationwide within the United States
Status
Ongoing
Quantity
N/A
Lot / codes
a) Lot #: D2402186, Exp. Date 09/30/2026. b) Lot #: D2402019, Exp. Date 08/31/2026; D2402094, Exp. Date 09/30/2026; D2500022, D2500023, D2500021, Exp. Date 12/31/2026.
Company location
Raleigh, NC
Recall type
Voluntary: Firm initiated
Recall number
D-0779-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0779-2026 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.