WP Thyroid recalled over manufacturing violations

Recall date

August 25, 2020

Source

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

Official notice title

RLC Labs Inc. recalls WP Thyroid, Westhroid Pure, 1.25 Grain (81.25 mg) Thyroid USP packaged in a) 1,000 Tablets, NDC 64727-6050-2 ; b) 30 Ta…

Recall number

D-1610-2020

FDA classification

Class II

Brand / firm

RLC Labs Inc.

Sold / distributed

Nationwide in the United States

Why it was recalled

CGMP Deviations: manufactured under the same conditions as those found to be subpotent.

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

What was recalled

WP Thyroid, Westhroid Pure, 1.25 Grain (81.25 mg) Thyroid USP packaged in a) 1,000 Tablets, NDC 64727-6050-2 ; b) 30 Tablets, NDC 64727-6050-4; c) 60 Tablets, NDC 64727-6050-5; d) 90 Tablets, NDC 64727-6050-6; e) 100 Tablets, NDC 64727-6050-1; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034