Westminster Pharmaceuticals LLC recalls Levothyroxine and Liothyronine (Thyroid Tablets, USP), 2 grain (120 mg), 100-count bottles, Rx Only, Manufactured for: W
Recalled August 29, 2018 · FDA recall D-1182-2018 · Westminster Pharmaceuticals
Hazard
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. · FDA Class I
Units
Unknown
Sold at
Nationwide in the USA and Puerto Rico
Description
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.
Product
Levothyroxine and Liothyronine (Thyroid Tablets, USP), 2 grain (120 mg), 100-count bottles, Rx Only, Manufactured for: Westminster Pharmaceuticals, LLC, 154 Downing Street, Unit 1 & 2, Olive Branch, MS 38654, NDC 69367-158-04.
Manufacturer(s)
Westminster Pharmaceuticals LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →