Hydrocodone Bitartrate and Acetaminophen Tablets USP — Class II drug recall D-1053-2014
Terminated recall by Watson Laboratories Inc, reported 2014-02-05, distributed in AZ, CA, CT, FL, NV, OH, OK, PA…. Failed Tablet/Capsule Specifications; Product contains broken tablets.
| Recall number | D-1053-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Watson Laboratories Inc, Corona, CA, United States |
| Recall initiated | 2014-01-15 |
| Classified | 2014-01-30 |
| Reported by FDA | 2014-02-05 |
| Terminated | 2014-07-25 |
| Distributed | AZ, CA, CT, FL, NV, OH, OK, PA, SC, WI |
| Quantity | 717 bottles |
| NDC | 00591-0517-01 |
| Lot numbers | 697316A |
| Expiration dates | 2015-03-20 |
Product
Hydrocodone Bitartrate and Acetaminophen Tablets USP, CIII, 10 mg/ 660 mg, 100 count bottles, Rx only. Manufactured by Watson Laboratories, Inc., Corona, CA 92880. Distributed by: Watson Pharma, Inc. NDC: 00591-0517-01.
Reason for recall
Failed Tablet/Capsule Specifications; Product contains broken tablets.
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-1053-2014. 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.