Humulus 6X — Class II drug recall D-0866-2021
Terminated recall by Washington Homeopathic Products, Inc., reported 2021-10-06, distributed nationwide. Out-of-specification test results obtained for identification testing based on HPTLC analysis.
| Recall number | D-0866-2021 |
|---|---|
| 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 | 2021-08-20 |
| Classified | 2021-09-29 |
| Reported by FDA | 2021-10-06 |
| Terminated | 2022-06-21 |
| Distributed | Nationwide (US) |
| Quantity | 2 bottles |
| UPC / GTIN / UDI-DI | 00740640339695 |
| Lot numbers | 29298 |
| Expiration dates | 2026-08-17 |
Product
Humulus 6X, 15X, Sucrose/Lactose Pills, 6X Packaged as a) 4dr, UPC 7 40640 33969 5; 15X Packaged as b) 4 dr; WHP Homeopathic Medicine. Washington Homeopathic Products, 260 JR Hawvermale Way, Berkeley Springs, WV 25411.
Reason for recall
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
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-0866-2021. 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.