Food Recall Check
Class I · High risk Terminated Initiated Apr 5, 2017 (10 years ago)

Oberlander Bakery Gluten Free Brand Chocolate Kokosh Cake recall

Recalled by Oberlander Baking Co · Belleville, NJ, United States

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

Why it was recalled

Oberlander Gluten Free Brand Chocolate Kokosh Cake chocolate filled cake may contain undeclared almond.

Undeclared allergens: Tree nuts 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

Oberlander Bakery Gluten Free Brand Chocolate Kokosh Cake Net Wt. 16 oz. Manufactured by: Orthodox Baking Co. Inc. Belleville, NJ 07109, UPC 43711 18093 7

Quantity: 187 cartons

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.

last date sale of April 30

Where it was sold

California Florida Illinois Maryland New Jersey New York

FDA's distribution note: CA, FL , MD, IL, NJ and NY

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 tree nuts, 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
Oberlander Baking Co
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 5, 2017
In FDA report of
May 24, 2017
Terminated
Aug 22, 2017
FDA recall number
F-2221-2017 · event 76960
Official record
FDA enforcement report search

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