FDAClass I · Food · Recall H-1388-2026 · Recalled September 23, 2026

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

Agency report date: September 23, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: Mon Sire Brie
Company / brand: Optimus d/b/a/ Markys Caviar
Lot / serial / date codes: LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026
Distribution: Florida

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Mon Sire Brie recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: H-1388-2026
Brand: All Optimus d/b/a/ Markys Caviar recalls
Classification: Class I
Units affected: 22 cases (44 units)
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

Mon Sire Brie recall status

Companies & origin

Recalling firm location: Miami Gardens, FL, United States
Firm address: 1000 Nw 159th Dr, N/A, 33169-5806

Identifying details (verbatim from the notice)

Product codes / lots: LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026
Distribution: Florida
Firm notified the public via: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID: 99841
Recall initiated: August 25, 2026
FDA classified: September 17, 2026
FDA report date: September 23, 2026

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Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
NHTSA — vehicles, car seats, tires ↗ (aggregated here; use NHTSA's VIN lookup to check a specific vehicle)
FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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