Food Recall Check
Class I · High risk Terminated Initiated Jul 30, 2019 (7 years ago)

Door County Whitefish Smoked Whitefish Pate recall

Recalled by Ruleau Bros, Inc. · Stephenson, MI, United States

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

Why it was recalled

Undeclared Anchovy, Egg, Soy

Undeclared allergens: Egg Soy Fish

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

Door County Whitefish Smoked Whitefish Pate 8oz plastic tub UPC 8 55356 00402 4 Keep Refrigerated 12 retail units per wholesale case

Quantity: 250 cases; 3000 retail units

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 numbers: 19126, 19105, 29029, 19093 Expiration dates: 8/2/19, 8/9/19, 8/16/19, 8/23/19

Where it was sold

Illinois Michigan

FDA's distribution note: Single distributor in IL, six retailers in MI, and direct sales to consumers at a local farm market in Michigan

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, soy, fish; 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
Ruleau Bros, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 30, 2019
In FDA report of
Aug 28, 2019
Terminated
Nov 3, 2020
FDA recall number
F-2079-2019 · event 83481
Official record
FDA enforcement report search