ACCORD HEALTHCARE Recalls Levothyroxine Sodium Tablets
This is a Class II recall. This product may cause temporary health problems or pose a slight threat of a serious nature.
ACCORD HEALTHCARE Recalls Levothyroxine Sodium Tablets
ACCORD HEALTHCARE, INC. · Class II — Moderate Risk

Product Description
Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg), 90 Tablets bottles, Rx only, Manufactured for: Accord Healthcare, Inc., Raleigh, NC 27617, Manufactured by: lntas Pharmaceuticals Limited, Camp Road, Selaqui, Dehradun-248 197, INDIA, NDC 16729-458-15.
Reason for Recall
Subpotent Drug
FDA Classification
Class II — Moderate Risk
A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
Distribution
US Nationwide.
Remedy
Consumers should stop using this product. Contact the recalling firm for further instructions regarding this product.
411 Press Analysis
A Class II FDA recall has been issued for a pharmaceutical product from ACCORD HEALTHCARE, INC., initiated on June 8, 2026. Subpotent Drug. This recall covers 6432 bottles, distributed in US Nationwide. While not the highest severity, consumers should exercise caution and stop using the product until the recall is resolved.
Sources: FDA openFDA Enforcement Database
This recall appears in: Drug & Medication Defects.