Food Recall Check
Class I · High risk Terminated Initiated Oct 2, 2012 (14 years ago)

Whole Foods Roasted Garlic Eggplant Soup recall

Recalled by Whole Foods Market Group Inc. · Everett, MA, United States

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

Why it was recalled

Product labeled as Whole Foods Roasted Garlic and Eggplant Soup may contain Lobster Corn Bisque. Undeclared allergens: Shellfish, Milk

Undeclared allergens: Milk Shellfish

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 Roasted Garlic Eggplant Soup , 24oz plastic container UPC: 3640630269

Quantity: 360/24 oz

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: October 04 2012

Where it was sold

Connecticut Massachusetts Maine New Jersey New York Rhode Island

FDA's distribution note: Massachusetts, Rhode Island, Maine, Connecticut, New York and New Jersey

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, shellfish; 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
Whole Foods Market Group Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 2, 2012
In FDA report of
Oct 24, 2012
Terminated
Jun 1, 2015
FDA recall number
F-0290-2013 · event 63339
Official record
FDA enforcement report search

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