Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

R2103 Recalled by Washington Homeopathic Products, Inc. Due to CGMP Deviations: products were not manufactured under current...

Date: November 8, 2019
Company: Washington Homeopathic Products, Inc.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Washington Homeopathic Products, Inc. directly.

Affected Products

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.

Quantity: a) 1 bottle; b) 11 bottles

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Washington Homeopathic Products, Inc.

Washington Homeopathic Products, Inc. has 76 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report