D-1614-2020 Class I Terminated

Recalled by RLC Labs Inc. — Phoenix, AZ

Recall Details

Product Type
Drugs
Report Date
September 23, 2020
Initiation Date
August 25, 2020
Termination Date
November 8, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
N/A

Product Description

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

Reason for Recall

Subpotent Drug: FDA analysis found product to be subpotent

Distribution Pattern

Nationwide in the United States

Code Information

Lot #: 119142, Exp. Date 01/2022