Food Recall Check
Class I · High risk Terminated Initiated Jul 14, 2015 (11 years ago)

Dijon Mustard Potato Salad recall

Recalled by D & D Foods, Inc. · Omaha, NE, United States

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

Why it was recalled

Cups of macaroni salad are in tubs which declare the product to be potato salad and fail to disclose the presence of milk and wheat allergens.

Undeclared allergens: Milk 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

Dijon Mustard Potato Salad, NET WT 3 LB (1.36 kg)

Quantity: 110 cases

Food: 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.

Lot Code: 15177D, Best if Used By: JUL. 31, 2015

Where it was sold

Iowa Illinois Kansas Minnesota Missouri Nebraska South Dakota Wisconsin

FDA's distribution note: Product is sold exclusively in Hy-Vee retail grocery stores in Iowa, Illinois, Kansas, Minnesota, Missouri, Nebraska, South Dakota and Wisconsin.

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, 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
D & D Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 14, 2015
In FDA report of
Aug 19, 2015
Terminated
Oct 21, 2015
FDA recall number
F-2952-2015 · event 71705
Official record
FDA enforcement report search

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