D-0506-2020 Class II Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- November 27, 2019
- Initiation Date
- November 8, 2019
- Termination Date
- January 4, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- a) 1 bottle; b) 11 bottles
Product Description
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 Pattern
Product was distributed Nationwide throughout the United States, Canada and Saudi Arabia
Code Information
Lot #: 28557