Warfarin Sodium Tablets — Class III drug recall D-1584-2014
Terminated recall by Taro Pharmaceuticals U.S.A., Inc., reported 2014-09-24, distributed in CA, HI, IL, MS, NH, OH, TX. Failed Content Uniformity Specifications.
| Recall number | D-1584-2014 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY, United States |
| Recall initiated | 2014-08-25 |
| Classified | 2014-09-12 |
| Reported by FDA | 2014-09-24 |
| Terminated | 2018-05-18 |
| Distributed | CA, HI, IL, MS, NH, OH, TX |
| Quantity | 1,396 bottles |
| NDC | 51672-4027, 51672-4027-00, 51672-4027-01, 51672-4027-03, 51672-4027-07, 51672-4028, 51672-4028-00, 51672-4028-01, 51672-4028-03, 51672-4028-07, 51672-4029, 51672-4029-00, 51672-4029-01, 51672-4029-03, 51672-4029-07, 51672-4030, 51672-4030-00, 51672-4030-01, 51672-4030-03, 51672-4030-07, 51672-4031, 51672-4031-00, 51672-4031-01, 51672-4031-03, 51672-4031-07 and 18 more |
| Lot numbers | 149400, 149649 |
| Expiration dates | 2016-01-20 |
Product
Warfarin Sodium Tablets, USP Crystalline, 2 mg, 100 and 1000 Tablet Bottles, Rx Only. Mfd. by: Taro Pharmaceutical Industries, Ltd., Haifa Bay, Israel 26110. Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532. 100 Tablet Bottle NDC: 51672-4028-1, 1000 Tablet Bottle NDC: 51672-4028-3.
Reason for recall
Failed Content Uniformity Specifications.
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-1584-2014. 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.