# FDA recall D-0489-2024

> **RemedyRepack Inc.** · Class II · drug recall initiated 2024-05-02.

## 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

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0489-2024
- **Recalling firm:** RemedyRepack Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-05-02
- **Report date:** 2024-05-15
- **Termination date:** 2024-09-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Indiana, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0489-2024

## Citation

> AI Analytics. FDA recall D-0489-2024. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/D-0489-2024. Source: US FDA. Licensed CC0.

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