Food recall

Weleda Inc recall: Hepatodoron tablets

Weleda Inc, of Irvington, NY, recalled Hepatodoron tablets. The FDA's reason: “Dietary supplement may contain metal.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on April 4, 2023, and the FDA first listed it in its Enforcement Report of May 10, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Metal, plastic, glass or other objects

Status

Terminated

Closed December 13, 2023

The recall

Company
Weleda Inc (Irvington, NY)
Reason, in FDA's words
“Dietary supplement may contain metal”
Where it was sold
nationwide
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
92052

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0820-2023 Class II

    Hepatodoron tablets, 200 pcs

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

    Quantity: 890 units

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of May 10, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.