WIEBE DAIRY RAW MILK CHEESE Ingredients recall

Recalled by Paris Brothers Inc · Kansas City, MO, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Environmental samples positive for Listeria.

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

WIEBE DAIRY RAW MILK CHEESE Ingredients: Grade A Raw milk, salt, cheese culture, enzyme, annatto Cottonwood River RESERVE www.jasonwiebedairy.com Durham, KS 67438 Plant # 20-037 Carton Label (not available to consumers) ITEM ID: 02000002 PARIS BROTHERS, INC. 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4188 COTTONWOOD RIVER CHEDDAR 10 LB PC

Quantity: 2981 lbs (total)

Food: Cheese Milk & dairy

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot: 05062022 Sell By Date: 01/31/2023

Where it was sold

FDA's distribution note: One consignee is a wholesale warehouse. The remainder of the consignees are grocery stores and food service establishments.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Paris Brothers Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: May 24, 2022
In FDA report of: Jul 13, 2022
Terminated: Oct 24, 2022
FDA recall number: F-1420-2022 · event 90300
Official record: FDA enforcement report search

Also recalled with it (7 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Listeria May 24, 2022