FDA-PR2026-08-21CHEMICAL

Vitruvias Therapeutics Thyroid Tablets 30 mg recalled for super potency risk

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Vitruvias Thyroid Tablets recalled for super potency risk

Vitruvias Therapeutics is recalling one lot (504950) of Thyroid Tablets, USP 30 mg because testing found the tablets may contain higher-than-intended amounts of thyroid hormone. Taking overly potent thyroid medication can cause an overactive thyroid, leading to weight loss, rapid heartbeat, chest pain, and other serious symptoms, especially in elderly people, pregnant women, and infants.

  • Check if your Thyroid Tablets are from lot 504950 (expiration 9/30/2026).
  • Do not stop taking your medication without calling your doctor first—they can provide guidance or a replacement prescription.
  • Contact your healthcare provider if you have experienced symptoms like weight loss, rapid heartbeat, chest pain, or heat intolerance.
  • Call Vitruvias Therapeutics at (256) 239-9373 (Mon–Fri, 9 a.m.–5 p.m. CT) or email safety@vitruvias.com with questions about the recall.

Product photos

Thyroid Tablets USP Label
Thyroid Tablets USP Label
Hazard

AUBURN, Ala. (August 21, 2026) – Vitruvias Therapeutics, Inc. is voluntarily recalling one lot (Lot. No. 504950) of Thyroid Tablets, USP 30 mg to the consumer level. The product is being recalled because testing confirmed the potential for the product to be superpotent.

Who it affects
All ages
Illnesses reported
None reported

Official notice

https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/vitruvias-therapeutics-inc-issues-nationwide-recall-one-lot-thyroid-tablets-usp-30-mg-due-potential

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