Fresh Recalls

FDAClass III · Drug · Recall D-0840-2026 · Recalled September 9, 2026

Buprenorphine Sublingual Tablets (C-III) recall — American Health Packaging

Agency report date: September 9, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Buprenorphine Sublingual Tablets (C-III)
Company / brand
American Health Packaging
Lot / serial / date codes
Lot # 1030023, Exp Date: 06/30/2027.
Distribution
US Nationwide.
Agency product description and boundaries

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).

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Labeling: Label Mix-up

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class III: not likely to cause adverse health consequences.

Affected product: Buprenorphine Sublingual Tablets (C-III) recall status

3. Open the official notice or contact

Official recall ID
D-0840-2026
Brand
All American Health Packaging recalls
Classification
Class III
Units affected
10,953 cartons.
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Columbus, OH, United States
Firm address
2550 John Glenn Ave Ste A, N/A, 43217-1188

Identifying details (verbatim from the notice)

Product codes / lots
Lot # 1030023, Exp Date: 06/30/2027.
Distribution
US Nationwide.
Firm notified the public via
Letter
FDA event ID
99674
Recall initiated
August 19, 2026
FDA classified
September 14, 2026
FDA report date
September 9, 2026

Other drug recalls from around the same time

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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