Mon Sire Brie
Reason The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Face Rock Creamery Vampire Slayer Garlic Cheddar recall
Recalled by Frc INC · Bandon, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Face Rock Creamery Vampire Slayer Garlic Cheddar, net wt. 6oz. Ready to Eat, Refrigerated/ Perishable. Product is packaged in sealed in bag and shrink dipped. UPC 8 51222 00547 8. Face Rock Creamery, 680 2nd St. SE Bandon, OR 97411.
Quantity: 16/6oz units or 6lbs.
Food: Cheese
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Use By 110426.
Where it was sold
Oregon
FDA's distribution note: Distributed in Oregon only.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Frc INC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 14, 2025
- In FDA report of
- Dec 3, 2025
- Terminated
- Jan 9, 2026
- FDA recall number
- H-0212-2026 · event 97999
- Official record
- FDA enforcement report search
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