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FDA · Drug recall

Buprenorphine Sublingual Tablets (C-III)…

Sept. 9, 2026 Class 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.

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