Food Recall Check
Class I · High risk Terminated Initiated Apr 13, 2018 (8 years ago)

Formagere de la Brie recall

Recalled by Cheezwhse/Com · Armonk, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

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 brand, l 'Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g (8.8 oz), clear plastic package marked with lot # on the bottom, with UPC: 3 390010 004080.

Quantity: 22 cases

Food: Cheese Milk & dairy

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.

Lot Codes: H036, H038, H043, H044, H011

Where it was sold

Colorado Connecticut Maryland New Jersey New York Pennsylvania South Carolina Texas Utah Washington

FDA's distribution note: NY, NJ, CT, MD, UT, CO, SC, PA, TX and Washington D.C.

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
Cheezwhse/Com
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 13, 2018
In FDA report of
May 2, 2018
Terminated
Jun 4, 2018
FDA recall number
F-1136-2018 · event 79859
Official record
FDA enforcement report search

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