Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Levothyroxine and Liothyronine (Thyroid Tablets Recalled by Westminster Pharmaceuticals LLC Due to Failed Content Uniformity Specifications: Product was manufactured using...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Westminster Pharmaceuticals LLC directly.
Affected Products
Levothyroxine and Liothyronine (Thyroid Tablets, USP), 1/2 grain (30 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-155-04.
Quantity: Unknown
Why Was This Recalled?
Failed Content Uniformity Specifications: Product was manufactured using an adulterated active pharmaceutical ingredient; additionally, lack of process controls and good manufacturing practices resulted in finished product failing content uniformity specifications which can result in a product having a strength that is more or less than is labeled.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Westminster Pharmaceuticals LLC
Westminster Pharmaceuticals LLC has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report