FDA · Drug recall
Buprenorphine Sublingual Tablets (C-III)…
- Date
- Sept. 9, 2026
- Risk class
- Class III (FDA's definition, 21 CFR 7.3(m): a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences)
- Status
- Ongoing
- Filed by
- 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
- Distribution pattern
- US Nationwide.
- Quantity
- 10,953 cartons.
- Codes and lots
- Lot # 1030023, Exp Date: 06/30/2027.
- Recall started
- Aug. 19, 2026
- Recall number
- D-0840-2026
What should I do? Medicine recall: what to do
Source: FDA · Drug enforcement report, recall number D-0840-2026. The agency record governs; check it and the company before acting.