Carvedilol 25 mg — Class II drug recall D-0754-2021
Terminated recall by RemedyRepack Inc., reported 2021-09-01, distributed in FL, VA. A 500 count bottle of Carvedilol 25 mg tablets contained two Paroxetine Tablets, 40 mg. Product was repackaged
| Recall number | D-0754-2021 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RemedyRepack Inc., Indiana, PA, United States |
| Recall initiated | 2021-08-17 |
| Classified | 2021-08-20 |
| Reported by FDA | 2021-09-01 |
| Terminated | 2022-03-09 |
| Distributed | FL, VA |
| Quantity | 4 |
| NDC | 68382-0095-05, 70518-1826-01 |
| Lot numbers | B1273286-071521 |
| Expiration dates | 2022-07-31 |
Product
Carvedilol 25 mg, 180-count bottle, Rx only, Manufactured by Zydus Pharm, Pennington, NJ 08534, NDC 68382-0095-05, Repackaged by RemedyRepack Inc., Indiana, PA 15701, NDC 70518-1826-01
Reason for recall
A 500 count bottle of Carvedilol 25 mg tablets contained two Paroxetine Tablets, 40 mg. Product was repackaged into 180 count bottles.
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-0754-2021. 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.