Hepatodoron¿ tablets — Class II food recall F-0820-2023
Terminated recall by Weleda Inc, reported 2023-05-10, distributed nationwide. Dietary supplement may contain metal
| Recall number | F-0820-2023 |
|---|---|
| Product type | Food |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Weleda Inc, Irvington, NY, United States |
| Recall initiated | 2023-04-04 |
| Classified | 2023-05-04 |
| Reported by FDA | 2023-05-10 |
| Terminated | 2023-12-13 |
| Distributed | Nationwide (US) |
| Quantity | 890 units |
| Lot numbers | J033 |
| Expiration dates | 2027-01-31 |
Product
Hepatodoron¿ tablets, 200 pcs
Reason for recall
Dietary supplement may contain metal
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/F-0820-2023. 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.