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Class II · ModerateActive recall

Meclizine Hydrochloride

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

Does this affect you?
Check your lot numberLot #1024852; Exp 9/30/2026
Where it was soldU.S. Nationwide
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

Failed tablet specifications.

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 byAmerican Health Packaging
Brand nameMECLIZINE HYDROCHLORIDE
Generic nameMECLIZINE HYDROCHLORIDE
Active ingredient(s)MECLIZINE HYDROCHLORIDE
Distributed by / forAmerican Health Packaging, Columbus, Ohio, 43217
NDC60687-775-65
Show the full FDA record
Full product labelMeclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.
Recalling firmAmerisource Health Services LLC
DistributionU.S. Nationwide
Quantity697 cartons
Recall initiated2026-03-16
Report date2026-04-01
Recall completed—
Recall numberD-0418-2026
ClassificationClass II
FDA statusOngoing
Origin on fileColumbus OH 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.