Recall · openFDA Food Enforcement

Hepatodoron¿ tablets, 200 pcs: FDA Recall F-0820-2023

Agency action: Apr 4, 2023Record ID: F-0820-2023
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What happened

Original notice title

Hepatodoron¿ tablets, 200 pcs, recall F-0820-2023

From the archived source record

Dietary supplement may contain metal

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
Voluntary: Firm initiated
Report date
May 10, 2023
Termination date in the archive
Dec 13, 2023
Source checked
Jul 16, 2026
Record revision
09646a56d24f

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

Sources, dates, and coverage →

What is affected

Product
Hepatodoron¿ tablets, 200 pcs
Company
Weleda Inc
Lot / identifier
Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027
Market / distribution
nationwide