CLASS I Food recall · Reported 4 Jan 2023 · FDA Enforcement Report

Favorina Advent Calendar recalled by Lidl US TRADING

Lidl US Trading is recalling Favorina Advent Calendar, distributed nationwide in the US. The recall was initiated on 5 Dec 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBEST IF USED BY 2023
Quantity recalled10,524 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0208-2023
FDA event ID
91274
Recalling firm
Lidl US Trading, Arlington, VA
Classification
Class I
Status
Terminated
Recall initiated
5 Dec 2022
FDA classified
23 Dec 2022
Reported
4 Jan 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Chocolate

Timeline

5 Dec 2022Recall initiated by company
23 Dec 2022Classified by FDA+18 days
4 Jan 2023Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential Salmonella contamination.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Favorina Advent Calendar NET WT. 8.4OZ (240g) Premium Chocolate with a Creamy Filling UPC 4056489516965

Where it was distributed

Distributed throughout the US.

Nationwide

Stores named: Lidl

Questions about this recall

Why was it recalled?

Potential Salmonella contamination.

Which lots are affected?

BEST IF USED BY 2023

Where was it sold?

Distributed throughout the US.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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