Food Recall Check
Class I · High risk Terminated Initiated Jun 6, 2016 (10 years ago)

Waffle Works Double Chocolate Waffle Sandwich Snacks recall

Recalled by Herr Foods, Inc. · Nottingham, PA, United States

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

Why it was recalled

Packaging failed to declare the milk ingredient (whey powder) in the ingredient statement. The allergen statement listed Wheat and Soy Ingredients, but did not include Milk Ingredients (whey powder).

Undeclared allergens: Milk 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

Waffle Works Double Chocolate Waffle Sandwich Snacks Net Wt. 4 OZ.. Distributed By: Herr Foods, Inc., Nottingham, PA 19363. June0616 through February0117

Quantity: 84,528 packages

Food: Chocolate & candy Chips & snacks Salads, sandwiches & prepared foods

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.

June0616 through February0117

Where it was sold

Nationwide.

FDA's distribution note: Nationwide

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 milk, 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
Herr Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 6, 2016
In FDA report of
Jul 27, 2016
Terminated
Aug 15, 2017
FDA recall number
F-1700-2016 · event 74345
Official record
FDA enforcement report search

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