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Stop using now Food recall · FDA · Published April 13, 2018

Recall: Formagere de la Brie l'Explorateur Cheese Due to Listeria Risk

Cheezwhse/Com recalls Formagere de la Brie l'Explorateur soft ripened cheese due to potential Listeria monocytogenes contamination.

🇺🇸 FDA recall #F-1136-2018FoodFormagere de la Brie ›
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Recalling firmCheezwhse/Com111 Business Park Dr · Armonk, NY 10504-1708
✎ GovInfoNow plain-language explainer

What happened, in plain English

Cheezwhse/Com is recalling Formagere de la Brie brand, l'Explorateur, a soft ripened cheese made from pasteurized milk. The product may be contaminated with Listeria monocytogenes, which can cause serious illness. This is a Class I recall, indicating the highest risk of adverse health consequences. Read more at govinfonow.com/recall/19221-recall-formagere-de-la-brie-l-explorateur-cheese-due-to.

Source Summary by GovInfoNow · govinfonow.com/recall/19221-recall-formagere-de-la-brie-l-explorateur-cheese-due-to · Updated October 11, 2026 · FDA enforcement record: FDA #F-1136-2018

Cite this page

“Recall: Formagere de la Brie l'Explorateur Cheese Due to Listeria Risk.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19221-recall-formagere-de-la-brie-l-explorateur-cheese-due-to. Based on FDA recall #F-1136-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1136-2018%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacteria that can cause listeriosis, a serious infection. Infection can lead to fever, muscle aches, nausea, diarrhea, and in severe cases, meningitis or septicemia, particularly in vulnerable populations.

Who’s affected

Consumers in NY, NJ, CT, MD, UT, CO, SC, PA, TX and Washington D.C. who purchased the recalled cheese are affected. Individuals with weakened immune systems, pregnant women, older adults, and newborns are at the highest risk for serious infection from Listeria.

How to tell if you have this one

Check for Formagere de la Brie brand, l'Explorateur soft ripened cheese in 250g (8.8 oz) clear plastic packages. Look for lot codes H036, H038, H043, H044, or H011 on the bottom of the package and UPC 3 390010 004080.

  • Brand
    Formagere de la Brie
  • Product
    Formagere de la Brie brand, l 'Explorateur, soft ripened cheese made from pasteurized milk, product comes in a 250g
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled cheese as it may be contaminated with Listeria monocytogenes.

  2. Discard or return the item

    The record does not specify a remedy, so consumers should discard the product or contact the retailer for a refund if possible.

Where it went and when

Where it was distributed

Distributed in 9 states and D.C..

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: not listedCAUtah: yesUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “NY, NJ, CT, MD, UT, CO, SC, PA, TX and Washington D.C.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Colorado, Connecticut, District of Columbia, Maryland, New Jersey, New York, Pennsylvania, South Carolina, Texas, Utah.

Recall timeline

FDA terminated this recall 52 days after the firm started it.

1. Firm started the recall: Apr 13, 201812. FDA classified it Class I: Apr 26, 201823. Published in FDA’s Enforcement Report: May 2, 201834. FDA terminated the recall: Jun 4, 201842018
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1136-2018 (April 13, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1136-2018 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA