Desmopressin Acetate Tablets — Class III drug recall D-1235-2015
Terminated recall by American Health Packaging, reported 2015-07-22, distributed nationwide. Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
| Recall number | D-1235-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | American Health Packaging, Columbus, OH, United States |
| Recall initiated | 2015-06-26 |
| Classified | 2015-07-14 |
| Reported by FDA | 2015-07-22 |
| Terminated | 2018-08-15 |
| Distributed | Nationwide (US) |
| Quantity | 341 cartons |
| NDC | 68084-0606-21 |
| Lot numbers | 151360 |
| Expiration dates | 2016-12-31 |
Product
Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.
Reason for recall
Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
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-1235-2015. 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.