Levothyroxine recall by Major Pharmaceuticals
Analysis based on 12 articles · First reported Jul 24, 2026 · Last updated Jul 29, 2026
The recall may affect patient trust and lead to temporary supply disruptions. However, the impact is limited as the recall is Class II and alternatives are available.
KC Pharmaceuticals initiated a nationwide recall of levothyroxine sodium tablets on July 13, 2026, due to subpotency. The FDA classified it as a Class II recall on July 17. The recall covers multiple strengths in 100-tablet cartons and 10-tablet blister packs distributed by KC Pharmaceuticals and Cardinal Health. Patients are advised not to stop medication without consulting a healthcare provider.
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