CLASS I Food recall · Reported 16 Aug 2023 · FDA Enforcement Report
Fabrique' EN Corse Tomme Corse AU Lait DE Brebis***Antoine recalled
Estancia Holdings is recalling Fabrique' EN Corse Tomme Corse AU Lait DE Brebis***Antoine Ottavi Fromager***aFFINAGE 3, distributed in Oregon. The recall was initiated on 23 Jun 2023 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
- F-1383-2023
- FDA event ID
- 92641
- Recalling firm
- Estancia Holdings, Cumming, GA
- Brand
- Fabrique' EN
- Classification
- Class I
- Status
- Completed
- Recall initiated
- 23 Jun 2023
- FDA classified
- 8 Aug 2023
- Reported
- 16 Aug 2023
- 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
- Other
Timeline
| 23 Jun 2023 | Recall initiated by company | |
| 8 Aug 2023 | Classified by FDA | +46 days |
| 16 Aug 2023 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possible microbiological contamination, specifically 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
FABRIQUE' EN CORSE TOMME CORSE AU LAIT DE BREBIS***ANTOINE OTTAVI FROMAGER***aFFINAGE 3 A' 5 MOIS SARL Fromagerie Ottavi 20240 Ghisonaccia Corsica
Where it was distributed
Product was shipped to one customer in Oregon. Sole consignee was notified; therefore, press was not issued.
Questions about this recall
Why was it recalled?
Possible microbiological contamination, specifically Listeria monocytogenes.
Which lots are affected?
LOT#: VC349 BBD: 08/05/2023
Where was it sold?
Product was shipped to one customer in Oregon. Sole consignee was notified; therefore, press was not issued.
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 26 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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