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Class II · ModerateActive recall

Oxycodone Hydrochloride

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

Does this affect you?
Check your lot numberLots #: 1027932, Exp Date 06/30/2027, 1028360, Exp Date 08/31/2027
Where it was soldNationwide in the USA
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

Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.

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 nameOXYCODONE HYDROCHLORIDE
Generic nameOXYCODONE HYDROCHLORIDE
Active ingredient(s)OXYCODONE HYDROCHLORIDE
Distributed by / forAmerican Health Packaging, Columbus, Ohio 43217, Carton
NDC10702-018
Show the full FDA record
Full product labelOxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11
Recalling firmAmerisource Health Services LLC
DistributionNationwide in the USA
Quantity31,676 packages
Recall initiated2026-01-14
Report date2026-02-18
Recall completed
Recall numberD-0338-2026
ClassificationClass II
FDA statusOngoing
Origin on fileColumbus OH United States

Related

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.