Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2 uni
Summary
The FDA issued a Class I for Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and w by Optimus Inc. d/b/a/ Markys Caviar. Reason: The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes..
Details
Source
Food Recall
External ID
H-1388-2026
Action Date
2026-09-23
Status
Ongoing
Category
food
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
Lot/Code Info: LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026
Quantity Affected: 22 cases (44 units)
Reason for Recall
The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Distribution
Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2026-08-25
Company
Miami Gardens, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 54 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Optimus Inc. d/b/a/ Markys Caviar) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Optimus Inc. d/b/a/ Markys Caviar have FDA actions?
This is the only FDA action we have on record for Optimus Inc. d/b/a/ Markys Caviar in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1388-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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