Food Recall Check
Class I · High risk Terminated Initiated May 1, 2020 (6 years ago)

RITZ Cheese Cracker Sandwiches recall

Recalled by Mondelez Global Llc · East Hanover, NJ, United States

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

Why it was recalled

The firm is recalling a limited quantity of RITZ Cheese Cracker Sandwiches Family Size (21.6 oz. carton) product in the United States, because of undeclared peanut allergen.

Undeclared allergen: Peanut

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

RITZ Cheese Cracker Sandwiches , Family Size , (21.6 oz. carton)

Quantity: 9110 cases

Food: Cheese Chips & snacks 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.

UPC 0 44000 03826 7 Best by Dates 18SEP20 20SEP20 28SEP20 29SEP20 30SEP20 01OCT20 02OCT20

Where it was sold

FDA's distribution note: Product has been distributed thru out the United States

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 peanut; 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
Mondelez Global Llc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 1, 2020
In FDA report of
Jun 3, 2020
Terminated
Oct 20, 2023
FDA recall number
F-0960-2020 · event 85598
Official record
FDA enforcement report search

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