Food Recall Check
Class I · High risk Terminated Initiated Jul 15, 2020 (6 years ago)

Whole Foods Spinach Artichoke Dip recall

Recalled by Winter Gardens Quality Foods, Inc. · New Oxford, PA, United States

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

Why it was recalled

The product has been recalled due to undeclared (allergen) egg

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

Whole Foods Spinach Artichoke Dip ,4-12 oz containers, Lot # 248 Manufactured on 7/8/2020 Use By: 07/26/2020

Quantity: 71 cases (284 saleable units)

Food: Leafy greens & salads Sauces, dips & dressings

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 # 248 , Item Number 4142

Where it was sold

Maryland

FDA's distribution note: All 71 cases (284 saleable units) were shipped to Whole Foods Market Mid-Atlantic Distribution Center 1555 Cabin Branch Rd Landover, MD 20785

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
Winter Gardens Quality Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 15, 2020
In FDA report of
Aug 5, 2020
Terminated
Aug 10, 2021
FDA recall number
F-1046-2020 · event 86050
Official record
FDA enforcement report search

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