RLC Labs Inc. recalls WP Thyroid, Westhroid Pure, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg, Levothyroxine (T4) 19 mcg], pac…

Recall date

August 25, 2020

Source

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

Recall number

D-1614-2020

FDA classification

Class I

Brand / firm

RLC Labs Inc.

Sold / distributed

Nationwide in the United States

Why it was recalled

Subpotent Drug: FDA analysis found product to be subpotent

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

WP Thyroid, Westhroid Pure, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg, Levothyroxine (T4) 19 mcg], packaged in a) 30-count bottles (NDC 64727-5550-4), b) 90-count bottles (NDC 64727-5550-6), c) 100-count bottles (NDC 64727-5550-1), Rx only, Manufactured by: RLC Labs Phoenix, AZ 85024