WP Thyroid, Westhroid Pure, 1/2 Grain (32.5 mg) Thyroid USP [Liothyronine (T3) 4.5 mcg…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Subpotent Drug: FDA analysis found product to be subpotent

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

Recalling firm: RLC Labs Inc.
NDC code: 64727-5550-4
Origin: AZ, United States
Initiated by: Voluntary: Firm initiated
FDA recall number: D-1614-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.