Food Recall Check
Class I · High risk Terminated Initiated Jun 10, 2012 (14 years ago)

Flavored cheddar cheese recall

Recalled by Vauxner-USA, LLC · Bow, WA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product may be contaminated with Listeria monocytogenes.

Pathogen: 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

Flavored cheddar cheese, vacuum packed in weights ranging from 0.25-0.50 pounds, labeled and batch coded by firm. Cheese labeled in part: "Medium Cheddar Red Pepper with Onion & Garlic Pasteurized whole milk, salt, culture, vegetable rennet, spices. r-BST free.***GOLDEN GLEN CREAMERY 15098 Field Road Bow, WA 98232***887"

Quantity: 99 lbs

Food: Cheese

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.

"887" on primary label

Where it was sold

Oregon Washington

FDA's distribution note: Farmers markets in Washington State and retailers in Washington and Oregon.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Vauxner-USA, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 10, 2012
In FDA report of
Sep 12, 2012
Terminated
Jan 18, 2013
FDA recall number
F-2113-2012 · event 62282
Official record
FDA enforcement report search

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