Desmopressin Acetate Tablets — Class III drug recall D-1285-2015
Terminated recall by Actavis Laboratories, FL, Inc., reported 2015-08-12, distributed nationwide. Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.
| Recall number | D-1285-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Actavis Laboratories, FL, Inc., Davie, FL, United States |
| Recall initiated | 2015-06-23 |
| Classified | 2015-08-04 |
| Reported by FDA | 2015-08-12 |
| Terminated | 2016-12-30 |
| Distributed | Nationwide (US) |
| Quantity | 11,445 bottles |
| NDC | 00591-2464-01 |
| Lot numbers | 982021M |
| Expiration dates | 2016-12-20 |
Product
Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA; Distributed by Actavis Pharma, Inc. Parsippany, NJ 07054 USA. NDC: 0591-2464-01.
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-1285-2015. 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.