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Class I · Most seriousRecall completed

WP Thyroid

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot #: 119142, Exp. Date 01/2022
Where it was soldNationwide in the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Subpotent Drug: FDA analysis found product to be subpotent

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byRLC Labs Phoenix, AZ 85024
Distributed by / forRLC Labs Inc.
NDC64727-5550-4
Show the full FDA record
Full product labelWP 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 firmRLC Labs Inc.
DistributionNationwide in the United States
QuantityN/A
Recall initiated2020-08-25
Report date2020-09-23
Recall completed2023-11-08
Recall numberD-1614-2020
ClassificationClass I
FDA statusTerminated
Origin on filePhoenix AZ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.