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FDAFDA · Food and drugs·Recall number D-1614-2020

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

Published September 23, 2020 · Recall initiated: August 25, 2020

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Subpotent Drug: FDA analysis found product to be subpotent

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
RLC Labs Inc.
Distributor
Nationwide in the United States
Lot
Lot #: 119142, Exp. Date 01/2022
Risk classification
Class I
Area (FDA)
drug
Country
United States

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