American Health Packaging recalls Buprenorphine Sublingual Tablets
- Recalling company
- American Health Packaging
- Product
- 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).
- Reason
- Labeling: Label Mix-up
- Classification
- Class III – not likely to cause adverse health consequences
- Recall date
- Aug 19, 2026
- Reported
- Sep 9, 2026
- Distribution
- US Nationwide.
- Status
- Ongoing
- Quantity
- 10,953 cartons.
- Lot / codes
- Lot # 1030023, Exp Date: 06/30/2027.
- Company location
- Columbus, OH
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0840-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0840-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.