Nature-Throid 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 Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 mcg], 2.5 Grain (162.5 mg) Tablets, pa…

Recall number

D-1604-2020

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

Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 mcg], 2.5 Grain (162.5 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3310-4; b) 60-count bottles, NDC 64727-3310-5; c) 90-count bottles, NDC 64727-3310-6; d) 100-count bottles, NDC 64727-3310-1; and e) 1,000-count bottles, NDC 64727-3310-2; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034.