CLASS II ONGOING Drug recall · Reported 21 Oct 2026 · FDA Enforcement Report

Metoclopramide Tablets, USP, 5 mg (10 recalled

American Health Packaging is recalling Metoclopramide Tablets, USP, 5 mg (10 x, distributed nationwide in the US. The recall was initiated on 6 Oct 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 1028135, 1029555; Exp. Date 07/31/2027
NDC60687-620, 60687-631
Quantity recalled5,363 cartons

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0042-2027
FDA event ID
100100
Recalling firm
American Health Packaging, Columbus, OH
Manufacturer
American Health Packaging
Classification
Class II
Status
Ongoing
Recall initiated
6 Oct 2026
FDA classified
14 Oct 2026
Reported
21 Oct 2026
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

6 Oct 2026Recall initiated by company
14 Oct 2026Classified by FDA+8 days
21 Oct 2026Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Presence of Foreign Tablets/Capsules

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Metoclopramide 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

Where it was distributed

US Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Presence of Foreign Tablets/Capsules

Which lots are affected?

Lot 1028135, 1029555; Exp. Date 07/31/2027

Where was it sold?

US Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 27 Oct 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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