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Class II · ModerateActive recall

Levoxyl

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

Does this affect you?
Check your lot numberLot # 24W07, Exp: 11/30/2026
Where it was soldUS Nationwide and Puerto Rico
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: confirmed out-of-specification (OOS) assay during stability testing.

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 byMade in Austria
Brand nameLEVOXYL
Generic nameLEVOTHYROXINE SODIUM
Active ingredient(s)LEVOTHYROXINE SODIUM
Distributed by / forPfizer Inc., New York, NY 10017
NDC60793-859-10
Show the full FDA record
Full product labelLevoxyl (levothyroxine sodium tablets, USP), tablets, 175 mcg, 1000-count bottle, Rx only, Distributed by Pfizer Inc., New York, NY 10017, Made in Austria. NDC 60793-859-10
Recalling firmPfizer
DistributionUS Nationwide and Puerto Rico
Quantity134 1000-count bottles
Recall initiated2026-09-29
Report date2026-10-28
Recall completed—
Recall numberD-0051-2027
ClassificationClass II
FDA statusOngoing
Origin on fileManhattan NY United States

Related

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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.