Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, C
Summary
The FDA issued a Class III for Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Dist by American Health Packaging. Reason: Labeling: Label Mix-up.
Details
Source
Drug Recall
External ID
D-0840-2026
Action Date
2026-09-09
Status
Ongoing
Category
drug
Product Description
Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC#: 60687-481-21, (Individual Dose NDC: 60687-481-11).
Lot/Code Info: Lot # 1030023, Exp Date: 06/30/2027.
Quantity Affected: 10,953 cartons.
Reason for Recall
Labeling: Label Mix-up
Distribution
US Nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-19
Company
Columbus, OH
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 53 drug recalls issued in the same week, part of 66 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 III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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-0840-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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