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Class II · ModerateRecall completed

Thyroid

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot: A26450 Exp. 05/2019
Where it was soldNationwide.
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

CGMP Deviations: Recall notice received from supplier that Thyroid Powder has inconsistent levels of the active ingredients levothyroxine and liothyronine.

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

Distributed by / forHumco Holding Group, Inc
NDC0395-6580-43
Show the full FDA record
Full product labelThyroid, USP (Full Strength) Levothyroxine 112.1 mcg/grain Liothyronine 29.2 mcg/grain Active Pharmaceutical Ingredient Rx Only 1000 grams NDC 0395-6580-43 Packaged by: Humco Texarkana, TX 75501 USA
Recalling firmHumco Holding Group, Inc
DistributionNationwide.
Quantity10 kilograms
Recall initiated2018-08-28
Report date2018-10-24
Recall completed2020-05-07
Recall numberD-0024-2019
ClassificationClass II
FDA statusTerminated
Origin on fileTexarkana TX 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.