Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 23, 2024 (3 years ago)

Egg salad sandwich packaged in clamshell for individual sale recall

Recalled by The Coastal Companies DBA Hearn Kirkwood · Jessup, MD, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Tuna salad sandwich was mislabeled as an egg salad sandwich. There is an undeclared allergen of fish (Tuna).

Undeclared allergens: Egg 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

Egg salad sandwich packaged in clamshell for individual sale. 7.22oz (205g) UPC 766375938415

Quantity: 551 units

Food: Salads, sandwiches & prepared foods

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.

Use By Date of 03/23/2024

Where it was sold

District of Columbia Florida Massachusetts Maryland Michigan New Jersey New York Ohio Pennsylvania Virginia

FDA's distribution note: Product was sold to institutions, hospitals and retailers in DC, FL, MA, MD, MI, NJ, NY, OH, PA, VA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to egg, 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
The Coastal Companies DBA Hearn Kirkwood
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 23, 2024
In FDA report of
Apr 17, 2024
Terminated
Jul 23, 2024
FDA recall number
F-1132-2024 · event 94284
Official record
FDA enforcement report search

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