RecallRadar
FDA · FoodClass I

Optimus Inc. d/b/a/ Markys Caviar food recall: Mon Sire Brie

Listeria

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99841
Recall initiated
Aug 25, 2026
Classified by FDA
Sep 17, 2026
Posted in Enforcement Report
Sep 23, 2026
Recalling firm
Optimus Inc. d/b/a/ Markys Caviar
Firm location
Miami Gardens, FL, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Aug 25, 2026. FDA classified it 23 days later, on Sep 17, 2026. Distribution reported by FDA: Florida

Recalled products (1)

  • H-1388-2026 Class I Ongoing

    Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2 units each, Keep Refrigerated

    Codes / lots: LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026

    Quantity: 22 cases (44 units)

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 99841
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.