CLASS II Food recall · Reported 9 Aug 2023 · FDA Enforcement Report

belVita Breakfast Sandwich, Dark Chocolate Creme variety recalled

Mondelez Global is recalling belVita Breakfast Sandwich, Dark Chocolate Creme variety (8 - packages), distributed nationwide in the US. The recall was initiated on 3 Jul 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll Best When Used by Dates prior to and including February 25, 2024

Quantity recalled5581 Cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1360-2023
FDA event ID: 92668
Recalling firm: Mondelez Global, East Hanover, NJ
Classification: Class II
Status: Terminated
Recall initiated: 3 Jul 2023
FDA classified: 3 Aug 2023
Reported: 9 Aug 2023
Type: Voluntary: Firm initiated
Customers notified by: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category: Undeclared Peanuts
Product category: Ready Meals

Timeline

3 Jul 2023	Recall initiated by company
3 Aug 2023	Classified by FDA	+31 days
9 Aug 2023	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Mondelz Global LLC (Mondelz) has initiated a recall of various products - belVita Breakfast Sandwich Dark Chocolate Creme and belVita Breakfast Sandwich Cinnamon Brown Sugar with Vanilla Creme, because of undeclared peanut allergen due to cross contamination.

Product as listed by the FDA

belVita Breakfast Sandwich, Dark Chocolate Creme variety (8 - 14.08 oz packages)

Where it was distributed

The product was distributed to all 50 States.

Nationwide

Questions about this recall

Is belVita Breakfast Sandwich, Dark Chocolate Creme variety (8 - packages) recalled?

Yes. Mondelez Global recalled belVita Breakfast Sandwich, Dark Chocolate Creme variety (8 - packages) on 3 Jul 2023. The recall is Class II and its status is Terminated. Recall number F-1360-2023.

Why was it recalled?

Which lots are affected?

All Best When Used by Dates prior to and including February 25, 2024

Where was it sold?

The product was distributed to all 50 States.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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