# FDA recall D-0506-2020

> **Washington Homeopathic Products, Inc.** · Class II · drug recall initiated 2019-11-08.

## Product

R2103, Active Ingredients: Berberis Aquifolium 3x;  Borax 3; , Kreosotum 10X; Sepia 3x. Inactive ingredient: 28% dilution alcohol, packaged in a) 470 mL bottle and b) 1000 mL bottle; Manufactured for Wisconsin Pharmacal Company, By: Washington Homeopathic Products, Inc., 260 JR Hawvermale Way, Berkeley Springs, WV  25411.

## Reason for recall

CGMP Deviations: products were not manufactured under current good manufacturing practices.

## Distribution

Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia

## Key facts

- **Recall number:** D-0506-2020
- **Recalling firm:** Washington Homeopathic Products, Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2019-11-08
- **Report date:** 2019-11-27
- **Termination date:** 2023-01-04

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Berkeley Springs, WV, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0506-2020

## Citation

> AI Analytics. FDA recall D-0506-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0506-2020. Source: US FDA. Licensed CC0.

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