FDA Drug recall D-0840-2026
Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217…
- FDA Drug
- Class III
- ongoing
- Published 2026-09-09
On 2026-09-09 the FDA classified a Class III recall of Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed by: American Health Packaging, Columbus, Ohio 43217… by American Health Packaging, citing labeling: Label Mix-up.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0840-2026 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2026-08-19 |
| Published | 2026-09-09 |
| Last updated | 2026-09-23 05:30 UTC |
| Company | American Health Packaging |
| Distribution | US |
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
Identifiers
| ndc | 60687-481-11 |
|---|---|
| ndc | 60687-481-21 |
| ndc | 60687-492-11 |
| ndc | 60687-492-21 |
| code_info | Lot # 1030023, Exp Date: 06/30/2027. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-23 05:30 UTC. Current status: ongoing.
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All American Health Packaging recalls
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0840-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.