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Swiss American Inc Recall: Potential contamination with Listeria monocytogenes

United States

TerminatedClass I

Company
Swiss American Inc
Product
Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 04…
Recall date
September 30, 2022
Terminated
February 2, 2023
Source
FDA

Reason for recall

Potential contamination with Listeria monocytogenes

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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 041563 2701 cases All best by dates through 12/14/2022

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0118-2023
Event ID
90952
Status
Terminated
Classification
Class I
Company
Swiss American Inc
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
Quantity
2701 cases
Reason
Potential contamination with Listeria monocytogenes
Recall initiation date
September 30, 2022
Report date
November 9, 2022
Classification date
Not published in this source record
Termination date
February 2, 2023
Distribution pattern
Distributed to wholesale accounts in LA, ME, MO, NC, and NY.
UPC, lot, and code information
UPC 041563; All best by dates through 12/14/2022
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Swiss American Inc

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Louisiana 1
Maine 1
Missouri 1
North Carolina 1
New York 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.