Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 14, 2012 (14 years ago)

Christian Cheese Ranch Cheddar Made in Kingfisher recall

Recalled by Christian Cheese, LLC · Kingfisher, OK, United States

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

Why it was recalled

Undeclared Soy lecithin

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Christian Cheese Ranch Cheddar Made in Kingfisher, Oklahoma (405-375-6711) Ingredients: Pasteurized Milk, Culture, Rennet, Salt, and Ranch Dressing. 1 unit weighing approximately 0.6 lbs and plastic vacuum packed in plastic. 1 case is approximately 32 units weighing approximately 0.60 lbs each.

Quantity: Approximately 15-16 units

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.

No codes are used at the facility. All product made approximately on June 7, 2012.

Where it was sold

Colorado Oklahoma

FDA's distribution note: CO and OK

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. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. 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
Christian Cheese, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 14, 2012
In FDA report of
Jul 17, 2013
Terminated
Aug 15, 2013
FDA recall number
F-1647-2013 · event 62716
Official record
FDA enforcement report search

Also recalled with it (5 more products)

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

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