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Class II · ModerateActive recall

Metoclopramide

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

Does this affect you?
Check your lot numberLot 1028135, 1029555; Exp. Date 07/31/2027
Where it was soldUS 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

Presence of Foreign Tablets/Capsules

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 nameMETOCLOPRAMIDE
Generic nameMETOCLOPRAMIDE
Active ingredient(s)METOCLOPRAMIDE HYDROCHLORIDE
Distributed by / forAmerican Health Packaging, Columbus, Ohio 43217
Show the full FDA record
Full product labelMetoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. NDC Carton: 60687-620-01; NDC Unit Dose: 60687-620-11
Recalling firmAmerican Health Packaging
DistributionUS Nationwide
Quantity5,363 cartons
Recall initiated2026-10-06
Report date2026-10-21
Recall completed—
Recall numberD-0042-2027
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.