RecallHawk
Class I Recall

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

Lidl US TRADING

Summary

The FDA issued a Class I for Favorina Advent Calendar NET WT. 8.4OZ (240g) Premium Chocolate with a Creamy Fi by Lidl US TRADING. Reason: Potential Salmonella contamination..

Details

Source

Food Recall

External ID

F-0208-2023

Action Date

2023-01-04

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: BEST IF USED BY 2023

Quantity Affected: 10,524 units

Reason for Recall

Potential Salmonella contamination.

Distribution

Distributed throughout the US.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-05

Company

Lidl US TRADING

Arlington, VA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 18 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Lidl US TRADING has 15 FDA actions in our database, including 15 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Lidl US TRADING have FDA actions?

Lidl US TRADING has 15 FDA actions in our database, including 15 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0208-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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