---
title: American Health Packaging Issues Drug Recall for Metoclopramide Tablets
canonical: https://federalfeed.com/american-health-packaging-issues-drug-recall-for-metoclopramide-tablets/
published: '2026-10-29T23:41:29-04:00'
updated: '2026-10-29T23:41:29-04:00'
author: FederalFeed Staff
section: Medicine & Device Recalls
tags:
- FDA
source: Food and Drug Administration
source_url: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=100100
publisher: FederalFeed
attribution: Copyright FederalFeed. Quote with credit to FederalFeed and a link to the canonical URL above.
---

# American Health Packaging Issues Drug Recall for Metoclopramide Tablets

American Health Packaging is recalling Metoclopramide Tablets, USP, 5 mg, due to the presence of foreign tablets or capsules. The recall, classified as Class II, began on October 6, 2026, and is ongoing, affecting distribution across the United States. Details of the recall can be found in the FDA's weekly enforcement report [here](https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=100100).

---

### Press Release: Food and Drug Administration

*Published October 21, 2026. Reproduced in full from the [Food and Drug Administration](https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=100100).*

#### American Health Packaging drug recall

- Recalling company: American Health Packaging
- Classification: Class II (may cause temporary or reversible health problems)
- Recall numbers: D-0042-2027
- Status: Ongoing
- Distribution: US Nationwide
- Recall started: October 6, 2026

#### What was recalled

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

#### Why

Presence of Foreign Tablets/Capsules

This drug recall appears in the FDA's weekly enforcement report. Details: [FDA recall event 100100](https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=100100).

Source: [Food and Drug Administration](https://www.accessdata.fda.gov/scripts/ires/index.cfm?Event=100100)