Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 8, 2015 (11 years ago)

Sugar Old Fashioned Gourmet Cookie Dough recall

Recalled by Tower Cafe Inc. DBA Okarche Bakery · Okarche, OK, United States

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

Why it was recalled

Undeclared soy and wheat in frozen cookie dough.

Undeclared allergens: Soy Wheat

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

Sugar Old Fashioned Gourmet Cookie Dough NET WT. 3 lb. (48 oz.) Distributed By: Tower Cafe, Okarche, OK 73762 packaged in plastic tub.

Quantity: 480 tubs

Food: Bread & bakery

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.

Product does not contain lot codes or best by dates. Recall applies to all product on the market. UPC: 025405737733

Where it was sold

Oklahoma

FDA's distribution note: Oklahoma.

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, wheat; 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
Tower Cafe Inc. DBA Okarche Bakery
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 8, 2015
In FDA report of
Dec 2, 2015
Terminated
Aug 24, 2016
FDA recall number
F-0225-2016 · event 72159
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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

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