Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 18, 2021 (5 years ago)

JUST Egg Inspired by America Roasted Potato recall

Recalled by Cuisine Solutions · Sterling, VA, United States

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

Why it was recalled

Undeclared egg and milk

Undeclared allergens: Milk 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

JUST Egg Inspired by America Roasted Potato, Dill, Chives, Red Bell Pepper, Black Pepper 4 Sous Vide Plant Egg Bites NET WT8.4OZ (238g). UPC: 0504402503, Expiration dates 2/22/2022, 3/1/2022, 3/8/2022, 2/22/2022, and 4/6/2022. 16 cartons per corrugated case, Carton GTIN 7 05044 02503 2, Case Bar Code 10 7050 440 25039

Quantity: 4633 cases

Food: Spices & seasonings

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.

82530, 82625, 82769, and 83367

Where it was sold

Nationwide.

FDA's distribution note: Distributed nationwide

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 milk, 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
Cuisine Solutions
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 18, 2021
In FDA report of
Jul 7, 2021
Terminated
Mar 30, 2022
FDA recall number
F-0743-2021 · event 88143
Official record
FDA enforcement report search

Also recalled with it (3 more products)

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

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