Vanilla Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz
Summary
The FDA issued a Class I for Vanilla Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. by Belgian Yummies. Reason: Undeclared Allergen: milk, eggs, wheat, peanuts, and tree nuts..
Details
Source
Food Recall
External ID
F-1230-2024
Action Date
2024-05-15
Status
Terminated
Category
food
Product Description
Vanilla Ice Cream Cookie Sandwich. Sandwiches packaged in a gold or clear bags. 50 sandwiches per case and weighting 4oz each sandwich.
Lot/Code Info: No lot numbers provided; Expiration date is 6 months from production date.
Quantity Affected: 1208.
Reason for Recall
Undeclared Allergen: milk, eggs, wheat, peanuts, and tree nuts.
Distribution
The products were only distributed in the state of Florida.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-03-20
Company
Fort Myers, FL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Belgian Yummies has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Belgian Yummies) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Belgian Yummies have FDA actions?
Belgian Yummies has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1230-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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