Food Recall Check
Class I · High risk Terminated Initiated Jan 28, 2022 (5 years ago)

Wishbone Chunky Blue Cheese Dressing recall

Recalled by Conagra Brands · Chicago, IL, United States

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

Why it was recalled

Undeclared eggs

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

Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-41321-00691-3; six bottles per case

Quantity: 200 cases

Food: Cheese 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: 4254201320 NOV0922

Where it was sold

Nationwide.

Arkansas Colorado Connecticut Iowa Indiana Kansas Kentucky Louisiana Michigan New Jersey New York Ohio Oklahoma Pennsylvania Texas Virginia

FDA's distribution note: Nationwide retailer distribution centers in Arkansas, Colorado, Connecticut, Iowa, Indiana, Kansas, Kentucky, Louisiana, Michigan, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Texas, and Virginia.

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
Conagra Brands
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 28, 2022
In FDA report of
Feb 16, 2022
Terminated
Feb 7, 2024
FDA recall number
F-0732-2022 · event 89506
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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