Exact FDA event identifier

Event 92052

1 recalled-product record grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: April 04, 2023
Product types: Food
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Weleda Inc

Dossier provenance

Source snapshots represented here

openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 1

Hepatodoron¿ tablets, 200 pcs

F-0820-2023

Recall number: F-0820-2023
Initiated: April 04, 2023
Classification: Class II
Status: Terminated
Recalling firm: Weleda Inc
Quantity: 890 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Dietary supplement may contain metal

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Dietary supplement may contain metal

Code information

Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027

Distribution pattern

nationwide