Thyroid recalled over manufacturing violations

Recall date

August 28, 2018

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Official notice title

Humco Holding Group, Inc recalls Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only…

Recall number

D-0023-2019

FDA classification

Class II

Brand / firm

Humco Holding Group, Inc

Sold / distributed

Nationwide.

Why it was recalled

CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Thyroid, USP (Porcine) Levothyroxine 36.3 mcg/grain Liothyronine 9.7 mcg/grain Active Pharmaceutical Ingredient Rx Only 100 grams NDC 0395-8077-62 Packaged by: Humco Texarkana, TX 75501 USA