Weleda Inc Recall: Dietary supplement may contain metal
United States
TerminatedClass II
- Company
- Weleda Inc
- Product
- Hepatodoron¿ tablets, 200 pcs
- Recall date
- April 4, 2023
- Terminated
- December 13, 2023
- Source
- FDA
Reason for recall
Dietary supplement may contain metal
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Hepatodoron¿ tablets, 200 pcs | Not published in this source record | 890 units | Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027 |
Distribution
- nationwide
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0820-2023
- Event ID
- 92052
- Status
- Terminated
- Classification
- Class II
- Company
- Weleda Inc
- Product description
- Hepatodoron¿ tablets, 200 pcs
- Quantity
- 890 units
- Reason
- Dietary supplement may contain metal
- Recall initiation date
- April 4, 2023
- Report date
- May 10, 2023
- Classification date
- Not published in this source record
- Termination date
- December 13, 2023
- Distribution pattern
- nationwide
- UPC, lot, and code information
- Art.-No. 00326500/003265xx Batch no: J033 Expiry date: January 31, 2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Weleda Inc
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
Official guidance and record verification
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How to interpret this historical record
This record is preserved as published by FDA, as of December 13, 2023.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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