SOFT RIPENED CHEESE - DOUBLE CREME BRIE D'AMIR Imported by Epicure Foods Corp. Flanders NJ, 07836 INGREDIENTS: Pasteu
Summary
The FDA issued a Class II for SOFT RIPENED CHEESE - DOUBLE CREME BRIE D'AMIR Imported by Epicure Foods Corp. by Paris Brothers Inc. Reason: Environmental samples positive for Listeria..
Details
Source
Food Recall
External ID
F-1421-2022
Action Date
2022-07-13
Status
Terminated
Category
food
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
Lot/Code Info: Lot: 05052022 Exp Date:6/9/22
Quantity Affected: 2981 lbs (total)
Reason for Recall
Environmental samples positive for Listeria.
Distribution
One consignee is a wholesale warehouse. The remainder of the consignees are grocery stores and food service establishments.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-24
Company
Kansas City, MO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 53 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Paris Brothers Inc has 8 FDA actions in our database, including 8 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Paris Brothers Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Paris Brothers Inc have FDA actions?
Paris Brothers Inc has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1421-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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