FDA recall record

Paris Brothers SOFT RIPENED CHEESE - DOUBLE CREME BRIE D'AMIR Imported by recall — FDA F-1421-2022

Environmental samples positive for Listeria.

Class IIclassification
F-1421-2022official record ID
Jul 13, 2022report date

Recall record at a glance

Official recordF-1421-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmParis Brothers Inc.
Report dateJul 13, 2022
Recall initiation dateMay 24, 2022
Quantity2981 lbs (total)
LocationKansas City, MO, United States

Official product description

SOFT RIPENED CHEESE - DOUBLE CREME BRIE D'AMIR Imported by Epicure Foods Corp. Flanders NJ, 07836 INGREDIENTS: Pasteurized Milk, Salt, Lactic Ferments, Enzymes, Ripening Cultures. PRODUCT OF FRANCE Carton Label (not available to consumers): ITEM ID: 02050003 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4186 BRIE D'AMIR 60% 1 KG HAND WRAP RW UPC: 033954-250528 ITEM ID: 02070236 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4186 BRIE D'AMIR 60% 3 KG HAND WRAP RW UPC: 033954-250535

Why the product was recalled

Environmental samples positive for Listeria.

Distribution information

One consignee is a wholesale warehouse. The remainder of the consignees are grocery stores and food service establishments.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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