FDAFDA · Food and drugs·Recall number D-0506-2020
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.
Published November 27, 2019 · Recall initiated: November 8, 2019
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
CGMP Deviations: products were not manufactured under current good manufacturing practices.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Washington Homeopathic Products, Inc.
- Distributor
- Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia
- Lot
- Lot #: 28557
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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