Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 4, 2023 (4 years ago)

Hepatodoron¿ tablets recall

Recalled by Weleda Inc · Irvington, NY, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Dietary supplement may contain metal

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Hepatodoron¿ tablets, 200 pcs

Quantity: 890 units

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

Nationwide.

FDA's distribution note: nationwide

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Weleda Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 4, 2023
In FDA report of
May 10, 2023
Terminated
Dec 13, 2023
FDA recall number
F-0820-2023 · event 92052
Official record
FDA enforcement report search

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