CLASS I Food recall · Reported 3 Sep 2025 · FDA Enforcement Report

Brie Royal Faucon recalled by Fromi U

Fromi U is recalling Brie Royal Faucon, distributed in New York. The recall was initiated on 11 Aug 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBatch Number 615
Quantity recalled52.911 lb

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-0547-2025
FDA event ID
97439
Recalling firm
Fromi U, New York, NY
Classification
Class I
Status
Terminated
Recall initiated
11 Aug 2025
FDA classified
28 Aug 2025
Reported
3 Sep 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Cheese

Timeline

11 Aug 2025Recall initiated by company
28 Aug 2025Classified by FDA+17 days
3 Sep 2025Published 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

Product may be contaminated with 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

Brie Royal Faucon; Net Weight about: 2.2lb/ 1kg LOT AUS/US

Where it was distributed

NY

New York

Questions about this recall

Why was it recalled?

Product may be contaminated with Listeria monocytogenes

Which lots are affected?

Batch Number 615

Where was it sold?

NY

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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