FDA Drug recall D-0506-2020
R2103, Active Ingredients: Berberis Aquifolium 3x
- FDA Drug
- Class II
- terminated
- Published 2019-11-27
On 2019-11-27 the FDA classified a Class II recall of R2103, Active Ingredients: Berberis Aquifolium 3x by Washington Homeopathic Products, citing CGMP Deviations: products were not manufactured under current good manufacturing practices.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0506-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-11-08 |
| Published | 2019-11-27 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Washington Homeopathic Products |
| Distribution | US |
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
CGMP Deviations: products were not manufactured under current good manufacturing practices.
Identifiers
| code_info | Lot #: 28557 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0506-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.