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

Lot, batch or date codesLOT#: VC349 BBD: 08/05/2023
Quantity recalled1cs/2/3kg wheels =13.5 lbs

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
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 2023Recall initiated by company
8 Aug 2023Classified by FDA+46 days
16 Aug 2023Published 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.

Oregon

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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