Strophanthus hisp 30X — Class II drug recall D-0889-2021
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-0889-2021 |
|---|---|
| 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 | 91 bottles |
| UPC / GTIN / UDI-DI | 00740640475539, 00740640475577, 00740640475652 |
| Lot numbers | 29061 |
Product
Strophanthus hisp 30X, Hives*, 20% Alcohol, Packaged in (a) 15 mL, UPC 7 40640 47553 9; (b) 30mL UPC 7 40640 47557 7; (c) 100mL, UPC 7 40640 47565 2; WHP Homeopathic Mecicine, 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-0889-2021. 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.