FlaggedRx← Medication recall checkHome
Class II · ModerateActive recall

Metoclopramide

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

Does this affect you?
Check your lot numberLot#: 5420094, Exp 09/30/2027
Where it was soldUSA 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 byTeva Pharmaceuticals USA, Inc.
Brand nameMETOCLOPRAMIDE
Generic nameMETOCLOPRAMIDE
Active ingredient(s)METOCLOPRAMIDE HYDROCHLORIDE
Distributed by / forTeva Pharmaceuticals, Parsippany, NJ 07054
NDC0093-2203-01
Show the full FDA record
Full product labelMetoclopramide Tablets, USP 10 mg, 100-count bottle, Rx only, Manufactured in Croatia by Pliva Hrvatska, d.o.o., Zageb, Croatia, Manufactured for Teva Pharmaceuticals, Parsippany, NJ 07054, NDC 0093-2203-01.
Recalling firmTeva Pharmaceuticals USA, Inc
DistributionUSA Nationwide
Quantity36612 cartons
Recall initiated2025-05-23
Report date2025-07-02
Recall completed—
Recall numberD-0473-2025
ClassificationClass II
FDA statusOngoing
Origin on fileParsippany NJ 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.