Independent register of U.S. FDA drug recalls · updated Nov 2, 2026
RxRecalls Get alerts
Class II · Moderate risk Ongoing Initiated Sep 29, 2026 (34 days ago)

Metoclopramide Tablets

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of Foreign Tablets/Capsules

Cause type: Particulate / foreign matter

Visible foreign particles - glass, metal, fibers or other material - found in the product. Particles can enter from equipment wear, containers or the process, and are dangerous in injectables. All particulate / foreign matter recalls.

What was 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

Affected NDCs 0093-2204-01 0093-2204-05

Compare with the code on your package — it is the most precise check available.

Drug: Metoclopramide

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Metoclopramide
NDC 00093-2204
HYDROCHLORIDE 5 mg/1 Tablet
Oral
Teva Pharmaceuticals USA, Inc. Rx
Recalling firm
Teva Pharmaceuticals USA, Inc
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0038-2027 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Metoclopramide recalls

See all

Other recalls by Teva Pharmaceuticals USA, Inc

All 2026 recalls