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Class III: unlikely to cause harmOngoing

American Health Packaging Buprenorphine Sublingual Tablets Recall

Buprenorphine Sublingual Tablets (C-III), 2 mg, 30 Tablets (3x10), Rx only, Distributed…

American Health Packaging · Columbus, OH

Risk level
Class III
Reported by FDA
Sep 9, 2026
Recall ID
D-0840-2026
Check your lot numberHow we source this data

Summary

American Health Packaging recalled Buprenorphine Sublingual Tablets starting Aug 19, 2026. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0840-2026 on Sep 9, 2026. Reason: Labeling: Label Mix-up. Status: Ongoing.

Why it was recalled

Labeling: Label Mix-up

Product description

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).

Lot numbers, UPCs & expiration codes

Lot # 1030023, Exp Date: 06/30/2027.

Where it was sold

US Nationwide.

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0840-2026
Classification
Class III
Status
Ongoing
Recall initiated
Aug 19, 2026
FDA report date
Sep 9, 2026
Quantity
10,953 cartons.
Recall type
Voluntary: Firm initiated
Recalling firm
American Health Packaging

Original FDA data

Every field from FDA enforcement report D-0840-2026, exactly as published.

Show all FDA fields
City
Columbus
State
OH
Status
Ongoing
Country
United States
Event ID
99674
Address
2550 John Glenn Ave Ste A
Code information
Lot # 1030023, Exp Date: 06/30/2027.
Postal code
43217-1188
Report date
Sep 9, 2026
Product type
Drugs
Recall number
D-0840-2026
Classification
Class III
Recalling firm
American Health Packaging
Product quantity
10,953 cartons.
Reason for recall
Labeling: Label Mix-up
Voluntary / mandated
Voluntary: Firm initiated
Product description
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).
Distribution pattern
US Nationwide.
Recall initiation date
Aug 19, 2026
Initial firm notification
Letter
Center classification date
Sep 14, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0840-2026, published Sep 9, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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