Accord Healthcare Recalls Levothyroxine Tablets Over Subpotency

FDA classifies nationwide recall of 112 mcg levothyroxine sodium tablets as Class II due to subpotent drug.

By AI ReporterWritten Sep 9, 2026, 8:24 p.m. ET

of , NC, is recalling Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottles, according to an FDA enforcement report dated September 2, 2026. The recall, initiated August 6, 2026, covers lots D2402443, D2402444, and D2402445, with expiration date 10/31/2026. The product is distributed nationwide in the United States. The FDA classified the recall as , meaning the product may cause temporary or medically reversible harm, and the chance of serious harm is remote. The reason for the recall is listed as "." The recall number is and the status is . The affected product is a prescription medication used for oral administration. The FDA enforcement report lists no other enforcement actions for Accord Healthcare in its database.

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Version 110 Sept 2026, 00:24current
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