Benzonatate Capsules — Class II drug recall D-0430-2015
Terminated recall by American Health Packaging, reported 2015-04-08, distributed nationwide. Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
| Recall number | D-0430-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Health Packaging, Columbus, OH, United States |
| Recall initiated | 2015-01-06 |
| Classified | 2015-04-01 |
| Reported by FDA | 2015-04-08 |
| Terminated | 2015-07-23 |
| Distributed | Nationwide (US) |
| NDC | 68084-0214, 68084-0214-01, 68084-0214-11 |
| Lot numbers | 145513 |
| Expiration dates | 2016-06 |
Product
Benzonatate Capsules, USP, 100 mg, 100 count (10X10), Rx only, Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217 --- NDC 68084-214-01(carton) NDC 68084-214-11 (individual dose)
Reason for recall
Failed Tablet/Capsule Specifications; recall initiated by manufacturer due to reports of wet capsules
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0430-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.