Goldenseal POWDER — Class I drug recall D-0220-2021
Terminated recall by Wishgarden Herbs, Incorporated, reported 2021-01-06, distributed nationwide. Microbial Contamination of a Non-Sterile Product: Product tested positive for Cronobacter Sakazakii.
| Recall number | D-0220-2021 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wishgarden Herbs, Incorporated, Louisville, CO, United States |
| Recall initiated | 2020-09-25 |
| Classified | 2021-01-07 |
| Reported by FDA | 2021-01-06 |
| Terminated | 2024-05-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, EG |
| Quantity | 298 jars |
| Reason classes | microbial contamination, sterility |
| Pathogens | cronobacter |
| UPC / GTIN / UDI-DI | 00656490641379 |
| Expiration dates | 2020-12, 2021-05, 2021-10, 2022-01, 2022-04 |
Product
Goldenseal POWDER, 0.25 oz. (7 g) plastic jars, WishGarden Herbs, Inc., Boulder, CO 80301. UPC 6 56490 64137 9
Reason for recall
Microbial Contamination of a Non-Sterile Product: Product tested positive for Cronobacter Sakazakii.
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-0220-2021. 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.