# FDA recall D-837-2013

> **Reumofan Plus USA** · Class I · drug recall initiated 2013-01-04.

## Product

Reumofan Plus, 30-count tablets per bottle, distriubted by Reumofan Plus USA, LLC and Reumofan USA, LLC, Springfield, PA, and manufactured by Riger Natural S.A., Mexico.

## Reason for recall

Marketed without an approved NDA/ANDA: Product may contain undeclared active pharmaceutical ingredients Diclofenac Sodium, Dexamethasone, and Methocarbamol.

## Distribution

Nationwide through internet sales.

## Key facts

- **Recall number:** D-837-2013
- **Recalling firm:** Reumofan Plus USA
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-01-04
- **Report date:** 2013-08-14
- **Termination date:** 2015-01-29

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-837-2013

## Citation

> AI Analytics. FDA recall D-837-2013. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/D-837-2013. Source: US FDA. Licensed CC0.

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