Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 22, 2016 (10 years ago)

7-Eleven Fresh to Go Sugar Cookie With M&m Chocolate Candy recall

Recalled by Dough Masters Co Inc · Warren, MI, United States

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

Why it was recalled

DOUGH MASTERS WHOLESALE BAKERY of Warren, MI. is recalling select 7-ELEVEN FRESH TO GO brand cookies because they may contain undeclared allergen peanuts resulting from a supplier's recall.

Undeclared allergen: Peanut

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

7-ELEVEN FRESH TO GO SUGAR COOKIE WITH M&M CHOCOLATE CANDY, 2 pieces, NET WT. 4 OZ. The affected cookies are packed in a clear, plastic film, two cookies per package.

Quantity: 1372 pieces

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.

Best By dates codes: Friday 0422, Saturday 0423, Sunday 0424, Monday 0425 on the front label; UPC 052548558765 Manhattan UPC: 052548558765.

Where it was sold

Michigan Ohio

FDA's distribution note: Domestic: Michigan & Ohio only

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 peanut; 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
Dough Masters Co Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 22, 2016
In FDA report of
Jun 15, 2016
Terminated
Mar 31, 2017
FDA recall number
F-1435-2016 · event 74024
Official record
FDA enforcement report search

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