FDA recall D-1614-2020

Product

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

Nationwide in the United States

Key facts

Status

Terminated

Initiation date

2020-08-25

Report date

2020-09-23

Termination date

2023-11-08

Voluntary/Mandated

Voluntary: Firm initiated

Location

Phoenix, AZ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1614-2020