FDA Recalls Thyroid Tablets Made by Chinese Firm

The U.S. Food and Drug Administration (FDA) announced the recall of Westminster Pharmaceuticals-made thyroid tablets due to the risk of adulteration.

The U.S. Food and Drug Administration (FDA) announced the recall of Westminster Pharmaceuticals thyroid tablets due to the risk of adulteration.

In an Aug. 9 statement, the FDA said that Levothyroxine and Liothyronine 15 mg, 30 mg, 60 mg, 90 mg, and 120 mg thyroid tablets are being recalled as precautionary measures.