Food Recall Check
Class I · High risk Terminated Initiated Apr 21, 2016 (10 years ago)

Chocolate Chunk Cookies prepared in store and sold in bakery… recall

Recalled by 7-Eleven, Inc. · Irving, TX, United States

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

Why it was recalled

Undeclared peanuts in fully-baked cookies.

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

Chocolate Chunk Cookies prepared in store and sold in bakery cases for self-service.

Quantity: Unknown

Food: Chocolate & candy 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.

No finished lot codes or UPC. Frozen 2.2 ounce puck manufacturer code: 1665630; UPC: 00471101711285 Mar/26/2017 Lot# 1000156705

Where it was sold

Missouri South Carolina Texas

FDA's distribution note: MO, SC, TX

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. 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
7-Eleven, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 21, 2016
In FDA report of
Sep 28, 2016
Terminated
Jan 17, 2017
FDA recall number
F-2339-2016 · event 73991
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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

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