Hydrocodone Bitartrate and Acetaminophen Tablets — Class III drug recall D-1061-2013
Terminated recall by Watson Laboratories Inc, reported 2013-09-25, distributed nationwide. Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may
| Recall number | D-1061-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Watson Laboratories Inc, Corona, CA, United States |
| Recall initiated | 2013-08-30 |
| Classified | 2013-09-17 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2014-07-25 |
| Distributed | Nationwide (US) |
| Quantity | 875 bottles |
| Reason classes | packaging |
| NDC | 00591-2611-05 |
| Lot numbers | 04/15, 706224A, 706225A |
Product
Hydrocodone Bitartrate and Acetaminophen Tablets, 7.5 mg/650 mg Tablets, 500 Count Bottle, Manufactured by: Watson Laboratories, Inc, Cocona, CA 92880, NDC 0591-2611-05.
Reason for recall
Defective Container: Defective bottles may not have tamper evident seals properly seated, and therefore it may be difficult to determine if the product had been opened or tampered with.
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-1061-2013. 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.