Hepatodoron Tablets (Weleda) – Metal contamination (2023)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hepatodoron¿ tablets, 200 pcs
Brand
Weleda Inc
Lot Codes / Batch Numbers
Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027
Products Sold
Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027
Weleda Inc is recalling Hepatodoron¿ tablets, 200 pcs due to Dietary supplement may contain metal. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Dietary supplement may contain metal
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026