Capecitabine 500 mg Tablet NDC 00378-2512-78 28 days supply and 21… — Class II drug recall D-0791-2018
Terminated recall by Kroger Specialty Pharmacy, Inc., reported 2018-05-16, distributed in AR, FL, IL, LA, MS. Lack of Processing Controls.
| Recall number | D-0791-2018 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kroger Specialty Pharmacy, Inc., Vicksburg, MS, United States |
| Recall initiated | 2018-04-03 |
| Classified | 2018-05-10 |
| Reported by FDA | 2018-05-16 |
| Terminated | 2020-05-07 |
| Distributed | AR, FL, IL, LA, MS |
| NDC | 00378-2512-78 |
Product
Capecitabine 500 mg Tablet NDC 00378-2512-78 28 days supply and 21 days supply
Reason for recall
Lack of Processing Controls.
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-0791-2018. 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.