CLASS I ONGOING Food recall · Reported 23 Sep 2026 · FDA Enforcement Report
Mon Sire Brie, soft-ripened French cheese recalled by Optimus
Optimus is recalling Mon Sire Brie, soft-ripened French cheese, distributed in Florida. The recall was initiated on 25 Aug 2026 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-1388-2026
- FDA event ID
- 99841
- Recalling firm
- Optimus, Miami Gardens, FL
- Brand
- Mon Sire
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 25 Aug 2026
- FDA classified
- 17 Sep 2026
- Reported
- 23 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Listeria
- Product category
- Cheese
Timeline
| 25 Aug 2026 | Recall initiated by company | |
| 17 Sep 2026 | Classified by FDA | +23 days |
| 23 Sep 2026 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Mon Sire Brie, soft-ripened French cheese, 1 kg, packed in carboard carton and wrapped in plastic parchment paper, 2 units each, Keep Refrigerated
Where it was distributed
Florida
Questions about this recall
Why was it recalled?
The firm was notified by their Brie Cheese supplier that sample results revealed the presence of Listeria monocytogenes.
Which lots are affected?
LOT 00000ZRAA1 EXP 08/15/2026 LOT 00000ZUAD2 EXP 08/18/2026
Where was it sold?
Florida
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 29 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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