Recall Ledger

Metoclopramide Tablets recall (Teva Pharmaceuticals USA, Inc)

DrugClass IIOngoing

Summary: Teva Pharmaceuticals USA, Inc is recalling Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC 100 Tablets: 0093-2204-01; NDC 500 Tablets: 0093-2204-05. Reason: Presence of Foreign Tablets/Capsules.

What is being recalled

Metoclopramide Tablets, USP, 5 mg, [100 or 500] Tablets per bottle, Rx Only, Manufactured for: Teva Pharmaceuticals, Parsippany, NJ 07054. NDC 100 Tablets: 0093-2204-01; NDC 500 Tablets: 0093-2204-05

Why

Presence of Foreign Tablets/Capsules

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US Nationwide.

How to tell if yours is affected

Lot, expiry: [100 Tablets] Lots 8634085, 8635085, 8636085, exp 07/2027; [500 Tablets] Lot 8633085, exp 07/2027

What to do

Check the product name, lot number and expiration date on your package against the codes above. If they match, do not stop taking a prescription medicine without talking to your doctor or pharmacist first; ask them about a replacement. Return or dispose of the product as your pharmacy advises.

Recall facts

Recall numberD-0038-2027
CategoryDrug
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedSeptember 29, 2026
ReportedOctober 21, 2026
CompanyTeva Pharmaceuticals USA, Inc
Company locationParsippany, NJ, United States
Initiated byVoluntary: Firm initiated
Quantity240,448 cartons

More recalls from Teva Pharmaceuticals USA, Inc · all drug recalls · recalls from September 2026

Official FDA record