TraMADol HCl 50 mg Tablet — Class II drug recall D-0489-2024
Terminated recall by RemedyRepack Inc., reported 2024-05-15, distributed nationwide. Presence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of
| Recall number | D-0489-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | RemedyRepack Inc., Indiana, PA, United States |
| Recall initiated | 2024-05-02 |
| Classified | 2024-05-08 |
| Reported by FDA | 2024-05-15 |
| Terminated | 2024-09-09 |
| Distributed | Nationwide (US) |
| Quantity | 23,970 tablets |
| NDC | 70518-3824-00, 70518-3824-02, 70518-3824-03 |
Product
TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: Advagen Pharma Limited, Plainsboro. NJ 08536, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, 724.465.8762
Reason for recall
Presence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of baclofen in a bottle of 1000-count tramadol
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-0489-2024. 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.