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CriticalFDAfda-F-0118-2023LACERATION

Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 041563 263709; Saint Louis Domestic Cut Brie Wedge, variable weight-6lb RD WT, ...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (laceration). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
2,701
Recall Date
September 30, 2022
Issuing Agency
Hazard
Laceration

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0118-2023.

Potential contamination with Listeria monocytogenes

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0118-2023.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Swiss American Inc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0118-2023.

Swiss American Inc

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Swiss American Inc Recall FAQ

Swiss American Inc is the subject of a food safety report: Saint Louis Domestic Brie Wedge, 7oz, saran wrapped, UPC: 041563 263709; Saint Louis Domestic Cut Brie Wedge, variable weight-6lb RD WT, .... The notice was published on September 30, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 2,701 units are potentially affected.