Drug recall D-0840-2026
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 for recall
Labeling: Label Mix-up
Lots and codes
Lot # 1030023, Exp Date: 06/30/2027.
Recall details
- Recalling firm
- American Health Packaging, Columbus, OH
- Quantity
- 10,953 cartons.
- Distribution
- US Nationwide.
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 19, 2026
Related products
- Buprenorphine – drug information
- NDC 60687-492 Buprenorphine · Buprenorphine Hydrochloride 8 mg/1 · American Health Packaging
- NDC 60687-481 Buprenorphine · Buprenorphine Hydrochloride 2 mg/1 · American Health Packaging