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FDAFDA · Food and drugs·Recall number D-1609-2020

WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP, packaged in a) 1,000 Tablets, NDC 64727-5750-2 ; b) 30 Tablets, NDC 64727-5750-4; c) 60 Tablets, NDC 64727-5750-5; d) 90 Tablets, NDC 64727-5750-6; e) 100 Tablets, NDC 64727-5750-1; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034

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

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

What to do

Voluntary: Firm initiated · E-Mail

Recall details

Manufacturer
RLC Labs Inc.
Distributor
Nationwide in the United States
Lot
All lots with expiry between 10/2020-07/2023
Risk classification
Class II
Area (FDA)
drug
Country
United States

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