RecallHawk
Class I Recall

Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 041563 263709; Saint Louis Domestic Cut Brie Wedge, variable w

Swiss American Inc

Summary

The FDA issued a Class I for Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 041563 263709; Saint L by Swiss American Inc. Reason: Potential contamination with Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-0118-2023

Action Date

2022-11-09

Status

Terminated

Category

food

Product Description

Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 041563 263709; Saint Louis Domestic Cut Brie Wedge, variable weight-6lb RD WT, saran wrapped, UPC: 041563 370018; Saint Louis Brie, variable weight, saran wrapped, UPC: 21107100000; Saint Louis CW Brie Wheel, 1/3 KG RD WT, saran wrapped, UPC: 00021171800000; Saint Louis Brie Pre Cut Wedges, 16 oz, UPC: 00021565000000, saran wrapped; TASTE OF INSPIRATION Double Creme Brie, variable weight, wedge, saran wrapped; TASTE OF INSPIRATION Double Creme Brie, 8 oz, wedge, UPC 72543999972, saran wrapped

Lot/Code Info: All best by dates through 12/14/2022

Quantity Affected: 2701 cases

Reason for Recall

Potential contamination with Listeria monocytogenes

Distribution

Distributed to wholesale accounts in LA, ME, MO, NC, and NY.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-09-30

Company

Swiss American Inc

Saint Louis, MO

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 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Swiss American Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Swiss American Inc have FDA actions?

This is the only FDA action we have on record for Swiss American Inc in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0118-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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