Formagere de la Brie
Reason The product may be contaminated with Listeria monocytogenes.
Formagere de la Brie FORMAGE FRANCAIS l'Explorateur recall
Recalled by Societe Fromagere de la Brie · St Simeon, N/A, France
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product may be contaminated with Listeria monocytogenes.
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
Formagere de la Brie FORMAGE FRANCAIS l'Explorateur, packaged in a plastic container, in 100g, 250g - UPC: 3 390010004080, and 1kg packages.
Quantity: 58 Cases
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.
All codes/expiration dates after February 10, 2019.
Where it was sold
FDA's distribution note: The cheeses are sold to importers in the USA.
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
- Societe Fromagere de la Brie
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 10, 2019
- In FDA report of
- May 1, 2019
- Terminated
- Apr 14, 2023
- FDA recall number
- F-1406-2019 · event 82655
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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