Food Recall Check
Class I · High risk Terminated Initiated Jun 7, 2022 (4 years ago)

Asparagus & Feta Sandwich packaged in 15" cellophane plastic recall

Recalled by Gourmondo Cafes & Catering · Seattle, WA, United States

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

Why it was recalled

Asparagus and Feta Sandwich is recalled due to undeclared eggs (allergens) in the sub-ingredient for mayonnaise.

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

Asparagus & Feta Sandwich packaged in 15" cellophane plastic, affixed with a label. Net Weight 11.04 oz. UPC code 859266007984.

Quantity: 21 units

Food: Cheese 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.

Product UPC code 859266007984 with best by dates of 6/5/2022 and 6/7/2022.

Where it was sold

Washington

FDA's distribution note: Product was distributed to retail stores in Washington.

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
Gourmondo Cafes & Catering
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 7, 2022
In FDA report of
Jun 29, 2022
Terminated
Aug 30, 2022
FDA recall number
F-1323-2022 · event 90402
Official record
FDA enforcement report search

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