FDA recall record
Hepatodoron¿ tablets, 200 pcs
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of December 13, 2023. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Hepatodoron¿ tablets, 200 pcs
Reason
Dietary supplement may contain metal
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Hepatodoron¿ tablets, 200 pcs
Code information listed by FDA
Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027
Distribution and firm information
Recalling firm listed by FDA: Weleda Inc
Firm location listed by FDA: Irvington, NY, United States
Distribution reported by FDA: nationwide
Product quantity listed by FDA: 890 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.