Optimus Inc. d/b/a/ Markys Caviar Recall: The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
United States
OngoingClass I
- Company
- Optimus Inc. d/b/a/ Markys Caviar
- Product
- Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in c…
- Recall date
- August 25, 2026
- Source
- FDA
Reason for recall
The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2 units each, Keep Refrigerated | Not published in this source record | 22 cases (44 units) | LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026 |
Distribution
- Florida
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-1388-2026
- Event ID
- 99841
- Status
- Ongoing
- Classification
- Class I
- Company
- Optimus Inc. d/b/a/ Markys Caviar
- Product description
- Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2 units each, Keep Refrigerated
- Quantity
- 22 cases (44 units)
- Reason
- The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
- Recall initiation date
- August 25, 2026
- Report date
- September 23, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Florida
- UPC, lot, and code information
- LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Optimus Inc. d/b/a/ Markys Caviar
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
