drugs LOW RISK Updated 2026-09-09

American Health Packaging recalls Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (

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Recalled 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).

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Hazard / Issue

Labeling: Label Mix-up

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot # 1030023, Exp Date: 06/30/2027.

✅ What Should You Do?

  1. 1Stop taking this medication and contact your doctor or pharmacist immediately.
  2. 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
  3. 3Check the lot number on your bottle or packaging against the recalled lots listed above.
  4. 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
View official government recall