R2103 — Class II drug recall D-0506-2020
Terminated recall by Washington Homeopathic Products, Inc., reported 2019-11-27, distributed nationwide. CGMP Deviations: products were not manufactured under current good manufacturing practices.
| Recall number | D-0506-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Washington Homeopathic Products, Inc., Berkeley Springs, WV, United States |
| Recall initiated | 2019-11-08 |
| Classified | 2019-11-18 |
| Reported by FDA | 2019-11-27 |
| Terminated | 2023-01-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, SA |
| Reason classes | cgmp |
| Lot numbers | 28557 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0506-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.