Food Recall Check
Class I · High risk Terminated Initiated Sep 16, 2021 (5 years ago)

Duke of Earle Spicy Chicken Sub recall

Recalled by The Earl of Sandwiches · Willernie, MN, United States

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

Why it was recalled

Sandwiches may contain undeclared soy and egg.

Undeclared allergens: Egg Soy

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

Duke of Earle Spicy Chicken Sub, Seasoned Chicken with Pepper Jack Cheese on Garlic Pepper French Bread. Net Wt. 7oz (198g), UPC 97256 19400, Keep Refrigerated. Earle of Sandwiches, Willernie, MN 55090

Quantity: 180 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.

Sandwiches Purchased before 9/15/2021

Where it was sold

Minnesota Utah Washington

FDA's distribution note: MN, UT, WA

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; 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
The Earl of Sandwiches
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 16, 2021
In FDA report of
Oct 13, 2021
Terminated
Apr 21, 2022
FDA recall number
F-0002-2022 · event 88744
Official record
FDA enforcement report search

Also recalled with it (4 more products)

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