belVita Breakfast Sandwich, Dark Chocolate Creme variety (192 - 2 lb 12 oz cartons per pallet)
Summary
The FDA issued a Class II for belVita Breakfast Sandwich, Dark Chocolate Creme variety (192 - 2 lb 12 oz carto by Mondelez Global Llc. Reason: Mondelz Global LLC (Mondelz) has initiated a recall of various products - belVita Breakfast Sandwich Dark Chocolate Creme and belVita Breakfast Sandwi.
Details
Source
Food Recall
External ID
F-1363-2023
Action Date
2023-08-09
Status
Terminated
Category
food
Product Description
belVita Breakfast Sandwich, Dark Chocolate Creme variety (192 - 2 lb 12 oz cartons per pallet)
Lot/Code Info: All Best When Used by Dates prior to and including February 25, 2024
Quantity Affected: 5004 Cases
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.
Distribution
The product was distributed to all 50 States.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-03
Company
East Hanover, NJ
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mondelez Global Llc has 13 FDA actions in our database, including 13 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Mondelez Global Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mondelez Global Llc have FDA actions?
Mondelez Global Llc has 13 FDA actions in our database, including 13 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1363-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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