Food Recall Check
Class I · High risk Terminated Initiated May 5, 2017 (9 years ago)

Wegmans Wegmans Family Pack Potato Salad recall

Recalled by ASK Foods Inc · Palmyra, PA, United States

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

Why it was recalled

Wegman's Potato Salad, Net Wt. 48 oz is being recalled for undeclared egg as the containers were labeled with a nutritional and ingredient statement from a different product.

Undeclared allergen: Egg

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

Wegmans Wegmans Family Pack Potato Salad, Net Wt. 48 OZ; Ingredients: Pasta Shells***Water, Cucumbers, Feta Cheese...ect; Allergens: Contains Milk and Wheat; Distributed By: Wegmans Food Markets, Inc., Rochester, NY 14603; Sell By: 5/7/17 3379-4; UPC: 7789024678

Quantity: 211 containers

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.

Sell By: 5/7/17 3379-4; UPC: 7789024678

Where it was sold

Massachusetts New York Pennsylvania

FDA's distribution note: MA, NY, PA

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 egg; 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
ASK Foods Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 5, 2017
In FDA report of
May 24, 2017
Terminated
Nov 27, 2017
FDA recall number
F-2240-2017 · event 77219
Official record
FDA enforcement report search

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