PEPPER JACK CHEESE Monterey Jack Cheese with Peppers Ingredients: Pasteurized Milk, Jalapeno Peppers, Cheese Culture,
Summary
The FDA issued a Class II for PEPPER JACK CHEESE Monterey Jack Cheese with Peppers Ingredients: Pasteurized by Paris Brothers Inc. Reason: Environmental samples positive for Listeria..
Details
Source
Food Recall
External ID
F-1426-2022
Action Date
2022-07-13
Status
Terminated
Category
food
Product Description
PEPPER JACK CHEESE Monterey Jack Cheese with Peppers Ingredients: Pasteurized Milk, Jalapeno Peppers, Cheese Culture, Salt, and Enzymes. DISTRIBUTED BY PARIS BROTHERS, INC. KANSAS CITY, MO 64161 UPC: 033954252256 Net wt. 1 LB(16OZ) 453G Carton Label (not available to consumers) ITEM ID: 02201809 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4189 PARIS BROTHERS PEPPER JACK 10-1 LB EW UPC: 033954252256
Lot/Code Info: Lot: 05042022 Exp Date: 11/5/22 BEST BY: 2022/11/04 or BEST BY: 2022/11/05
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-1426-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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