Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed by: American Health Packaging, Columbus,
Summary
The FDA issued a Class II for Metoclopramide Tablets, USP, 5 mg, 100 Tablets (10 x 10), Rx Only, Distributed b by American Health Packaging. Reason: Presence of Foreign Tablets/Capsules.
Details
Source
Drug Recall
External ID
D-0042-2027
Action Date
2026-10-21
Status
Ongoing
Category
drug
Product Description
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
Lot/Code Info: Lot 1028135, 1029555; Exp. Date 07/31/2027
Quantity Affected: 5,363 cartons
Reason for Recall
Presence of Foreign Tablets/Capsules
Distribution
US Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-10-06
Company
Columbus, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 39 drug recalls issued in the same week, part of 62 drug-related FDA actions this month.
American Health Packaging has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (American Health Packaging) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does American Health Packaging have FDA actions?
American Health Packaging has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0042-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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