Food Recall Check
Class I · High risk Terminated Initiated Dec 27, 2021 (5 years ago)

Macaroni & Cheese Macarrones con Queso recall

Recalled by Sandridge Food Corporation · Medina, OH, United States

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

Why it was recalled

Undeclared Egg Allergen

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

Macaroni & Cheese, Macarrones con Queso; 3-5 lb pouches/bolsas, NET WT/PESO NETO 240 OZ (15 LB) 6.80 kg; distributed by Gordon Food Service, Reorder No. 540061, Vendor Item # 4357505, Perishable. Keep Refrigerated. Perecedero. Mantener Refrigerado.

Quantity: 24 cases

Food: Cheese Pasta, rice & grains

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.

Best By 01/11/2022

Where it was sold

Texas

FDA's distribution note: Product was shipped to a Gordon Food Service in Texas. Gordon Food Service then distributed it to 3 restaurants and a hotel.

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
Sandridge Food Corporation
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 27, 2021
In FDA report of
Jan 12, 2022
Terminated
Jan 13, 2022
FDA recall number
F-0503-2022 · event 89313
Official record
FDA enforcement report search

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